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Feed Act

Content

Feed Act - content
Issuer:Riigikogu
Type:act
In force from:14.12.2019
In force until:31.12.2019
Translation published:19.12.2019

Feed Act1

Passed 11.01.2007
RT I 2007, 6, 32
Entry into force 01.02.2007

Amended by the following legal instruments (show)

PassedPublishedEntry into force
16.09.2009RT I 2009, 48, 32123.10.2009
22.04.2010RT I 2010, 21, 10701.01.2011 enters into force on the date which has been determined in the Decision of the Council of the European Union regarding the abrogation of the derogation established in respect of the Republic of Estonia on the basis provided for in Article 140 (2) of the Treaty on the Functioning of the European Union, Council Decision 2010/416/EU of 13 July 2010 (OJ L 196, 28.07.2010, p. 24-26).
22.04.2010RT I 2010, 22, 10801.01.2011 enters into force on the date which has been determined in the Decision of the Council of the European Union regarding the abrogation of the derogation established in respect of the Republic of Estonia on the basis provided for in Article 140 (2) of the Treaty on the Functioning of the European Union, Council Decision 2010/416/EU of 13 July 2010 (OJ L 196, 28.07.2010, p. 24-26).
15.09.2010RT I 2010, 72, 54215.10.2010
17.02.2011RT I, 02.03.2011, 104.03.2011
23.02.2011RT I, 25.03.2011, 101.01.2014; entry into force changed 01.07.2014 [RT I, 22.12.2013, 1]
19.06.2013RT I, 04.07.2013, 114.07.2013
05.12.2013RT I, 22.12.2013, 101.01.2014
19.02.2014RT I, 13.03.2014, 401.07.2014
05.06.2014RT I, 29.06.2014, 101.07.2014
12.06.2014RT I, 29.06.2014, 201.07.2014
19.06.2014RT I, 29.06.2014, 10901.07.2014, official titles of ministers replaced on the basis of subsection 107³ (4) of the Government of the Republic Act.
19.06.2014RT I, 12.07.2014, 101.01.2015
10.12.2014RT I, 30.12.2014, 101.01.2015
11.06.2015RT I, 30.06.2015, 401.09.2015, on the basis of subsection 107^4 (2) of the Government of the Republic Act the words 'Ministry of Agriculture' have been replaced with the words 'Ministry of Rural Affairs' in the appropriate case form.
31.05.2017RT I, 16.06.2017, 101.07.2017
14.06.2017RT I, 04.07.2017, 101.01.2018
25.10.2017RT I, 10.11.2017, 201.01.2018
20.02.2019RT I, 13.03.2019, 215.03.2019
20.11.2019RT I, 04.12.2019, 214.12.2019, the word ühenduseväline has been replaced with the word liiduväline in the appropriate case form in the Estonian wording of this Act.

Chapter 1 GENERAL PROVISIONS  

§ 1.  Scope of application of Act

 (1) This Act provides the requirements for feed, handling and use of feed and the requirements for organising state supervision over the compliance of feed with safety and other requirements in order to ensure the harmlessness thereof in terms of human and animal health and to the environment, and the favourable effect thereof on animals and animal products.

 (2) The provisions of the Administrative Procedure Act apply to administrative proceedings prescribed in this Act and in the legislation of the European Union, taking account of the specifications provided for in Regulation 2017/625 of the European Parliament and of the Council on official controls and other official activities performed to ensure the application of food and feed law, rules on animal health and welfare, plant health and plant protection products, amending Regulations (EC) No 999/2001, (EC) No 396/2005, (EC) No 1069/2009, (EC) No 1107/2009, (EU) No 1151/2012, (EU) No 652/2014, (EU) 2016/429 and (EU) 2016/2031 of the European Parliament and of the Council, Council Regulations (EC) No 1/2005 and (EC) No 1099/2009 and Council Directives 98/58/EC, 1999/74/EC, 2007/43/EC, 2008/119/EC and 2008/120/EC, and repealing Regulations (EC) No 854/2004 and (EC) No 882/2004 of the European Parliament and of the Council, Council Directives 89/608/EEC, 89/662/EEC, 90/425/EEC, 91/496/EEC, 96/23/EC, 96/93/EC and 97/78/EC and Council Decision 92/438/EEC (Official Controls Regulation) (OJ L 95, 07.04.2017, p. 1–142), in other legislation of the European Union and in this Act.
[RT I, 04.12.2019, 2 – entry into force 14.12.2019]

 (3) For the application of measures regarding feed, the minister responsible for the area may, within his or her competence, enact legislation regarding issues in which a Member State has the right to decide according to the legislation of the European Union.

§ 2.  Feed

 (1) For the purposes of this Act, feed means the substance or product as laid down in Article 3 (4) of Regulation (EC) No 178/2002 of the European Parliament and of the Council laying down the general principles and requirements of food law, establishing the European Food Safety Authority and laying down procedures in matters of food safety (OJ L 31, 01.02.2002, p. 1–24).

 (2) For the purposes of this Act, feed additives mean the feed additives as laid down in Article 2 (2) a) of Regulation (EC) No 1831/2003 of the European Parliament and of the Council on additives for use in animal nutrition (OJ L 268, 18.10.2003, p. 29–43).

 (3) For the purposes of this Act, premixture means the premixture as laid down in Article 2 (2) e) of Regulation (EC) No 1831/2003 of the European Parliament and of the Council.

 (4) For the purposes of this Act, feed materials mean the substances or products as laid down in Article 3 (2) g) of Regulation (EC) No 767/2009 of the European Parliament and of the Council on the placing on the market and use of feed, amending European Parliament and Council Regulation (EC) No 1831/2003 and repealing Council Directive 79/373/EEC, 82/471/EEC, 83/228/EEC, 93/74/EEC, 93/113/EEC and 96/25/EC, Commission Directive 80/511/EEC and Commission Decision 2004/217/EC (OJ L 229, 01.09.2009, p. 1–28).

 (5) For the purposes of this Act, compound feed means the feed as laid down in Article 3 (2) h) of Regulation (EC) No 767/2009 of the European Parliament and of the Council.

 (6) For the purposes of this Act, complete feed means the compound feed as laid down in Article 3 (2) i) of Regulation (EC) No 767/2009 of the European Parliament and of the Council.

 (7) For the purposes of this Act, complementary feed means the compound feed as laid down in Article 3 (2) j) of Regulation (EC) No 767/2009 of the European Parliament and of the Council.

 (8) For the purposes of this Act, mineral feed means the complementary feed as laid down in Article 3 (2) k) of Regulation (EC) No 767/2009 of the European Parliament and of the Council.

 (9) For the purposes of this Act, feed intended for particular nutritional purposes means the feed as laid down in Article 3 (2) o) of Regulation (EC) No 767/2009 of the European Parliament and of the Council.

 (10) For the purposes of this Act, medicated feed means the feed which contains veterinary medicinal products and which, because of its therapeutic and preventive characteristics is fed to animals without processing.
[RT I 2010, 72, 542 – entry into force 15.10.2010]

§ 3.  Assessment of guide to good practice

 (1) Compliance of the guide to good practice developed by the association of undertakings with the requirements of Article 21 (2) of Regulation (EC) No 183/2005 of the European Parliament and of the Council laying down requirements for feed hygiene (OJ L 35, 08.02.2005, p. 1–22), shall be assessed by the Veterinary and Food Board.

 (2) The Veterinary and Food Board refuses to approve the guide to good practice if the guide does not comply with the requirements as laid down in Article 21 (2) of Regulation (EC) No 183/2005 of the European Parliament and of the Council.

 (3) The Veterinary and Food Board submits the guide complying with the requirements as laid down in Article 21 (2) of Regulation (EC) No 183/2005 of the European Parliament and of the Council to the Ministry of Rural Affairs who shall forward it to the European Commission.

Chapter 2 REQUIREMENTS FOR FEED  

§ 4.  Compliance with requirements and harmlessness of feed

 (1) Feed shall comply with the requirements specified in the relevant legislation of the European Union, this Act and in the legislation established on the basis thereof.

 (2) Feed shall be harmless in terms of human and animal health and to the environment (hereinafter harmless) and in compliance with its intended purpose.

 (3) Feed shall not include a prohibited ingredient. For the purposes of this Act, prohibited ingredient means the material as laid down in Chapter 1 of Annex III to Regulation (EC) No 767/2009 of the European Parliament and of the Council.
[RT I 2010, 72, 542 – entry into force 15.10.2010]

 (4) Feed shall not include undesirable substance in higher quantities than permitted. For the purposes of this Act, an undesirable substance means the substance or product contained in a feed which is added, created or is present in a feed as a result of the manufacture process or as a result of environmental pollution, and the presence of which in feed in quantities larger than permitted may be harmful in terms of animal or human health or to the environment, or may harm the properties of animal products. Disease agents shall not be considered undesirable substances.

 (5) Feed which includes undesirable substance in higher quantities than permitted shall not be mixed with the same or other feed in order to decrease the content of undesirable substance.

 (6) The minister responsible for the area shall establish a list of undesirable substances and the maximum allowed quantities for the content thereof in feed.

 (7) If there is reason to believe that feed might be harmful in terms of human and animal health or to the environment or includes a prohibited ingredient (hereinafter harmful), the person who discovered such feed is immediately required to notify the Veterinary and Food Board thereof. Forwarded information shall be as accurate as possible and enable the commencement of supervision operations, setting out the location, origin and the operator of potentially harmful feed.

§ 5.  Labelling of feed

 (1) Feed shall be labelled in compliance with the requirements of Regulation (EC) No 767/2009 of the European Parliament and of the Council.

 (2) The labelling requirements for feed intended for particular nutritional purposes shall be established by the minister responsible for the area.

 (3) Upon the labelling of compound feed intended for pets, the name of the feed material included in compound feed may be replaced with the name of such feed material category.

 (4) The names and descriptions of feed material categories published on the labelling of compound feed for pets shall be established by the minister responsible for the area.

 (5) Feed containing, composed of or manufactured from genetically modified organisms shall be labelled in compliance with the requirements as laid down in Article 25 of Regulation (EC) No 1829/2003 of the European Parliament and of the Council on genetically modified food and feed (OJ L 268, 18.10.2003, p. 1–23) and in Articles 4 and 5 of Regulation (EC) No 1830/2003 of the European Parliament and of the Council concerning the traceability and labelling of genetically modified organisms and the traceability of food and feed products produced from genetically modified organisms (OJ L 268, 18.10.2003, p. 24–28).
[RT I 2010, 72, 542 – entry into force 15.10.2010]

Chapter 3 REQUIREMENTS FOR HANDLING AND USE OF FEED  

§ 6.  Handling and use of feed

 (1) The requirements specified in the relevant legislation of the European Union, this Act and other legislation established on the basis thereof shall be complied with upon handling and use of feed.

 (2) For the purposes of this Act, handling of feed means the activity related with feed in the stages of handling as laid down in Article 3 (16) of Regulation (EC) No 178/2002 of the European Parliament and of the Council.

 (3) For the purposes of this Act, the feed business operator means the person as laid down in Article 3 b) of Regulation (EC) No 183/2005 of the European Parliament and of the Council.

 (4) Premixtures and feed additives shall be transferred or delivered for other purpose only to the feed business operator who holds an activity licence for handling such premixtures or feed additives or who has submitted a notice of economic activities on the handling thereof.
[RT I, 25.03.2011, 1 – entry into force 01.07.2014 (entry into force changed – RT I, 22.12.2013, 1)]

 (5) The requirements of Annex III to Regulation (EC) No 183/2005 of the European Parliament and of the Council shall be complied with upon the use of feed for feeding to animals kept for the manufacture of foodstuffs of animal origin for putting into circulation.

 (6) Animal protein and feed containing animal protein shall be handled and used in compliance with the requirements as laid down in Regulation (EC) No 999/2001 of the European Parliament and of the Council laying down the rules for the prevention, control and eradication of certain transmissible spongiform encephalopathies (OJ L 147, 31.05.2001, p. 1–40), and in Regulation (EC) No 1069/2009 of the European Parliament and of the Council laying down health rules as regards animal by-products and derived products not intended for human consumption and repealing Regulation (EC) No 1774/2002 (OJ L 300, 14.11.2009, p. 1–33).
[RT I, 04.07.2013, 1 – entry into force 14.07.2013]

 (7) For the purposes of this Act, animal protein means the product as laid down in sub-clauses b) i-v of Chapter I and in sub-clauses a) i-iii of Chapter II to Annex IV of Regulation (EC) No 999/2001 of the European Parliament and of the Council.
[RT I, 04.07.2013, 1 – entry into force 14.07.2013]

 (8) The production of feed containing processed animal protein, dicalcium phosphate, tricalcium phosphate or blood products and feeding thereof to animals is allowed with the permission of the Veterinary and Food Board. The Veterinary and Food Board shall refuse to grant the permission if the undertaking fails to comply with the requirements specified in Regulation (EC) No 999/2001 of the European Parliament and of the Council.
[RT I, 04.07.2013, 1 – entry into force 14.07.2013]

 (9) The requirements on the content and format of the application for the permission specified in subsection (8) of this section shall be established by the minister responsible for the area.

 (10) The small quantities of primary production of feed and the requirements for placing thereof on the market shall be established by the minister responsible for the area.

§ 7.  Self-checking

 (1) A feed business operator whose undertaking engages in the activity as laid down in Article 5 (2) of Regulation (EC) No 183/2005 of the European Parliament and of the Council shall check the compliance of feed and the handling thereof (hereinafter self-checking) and apply measures in order to ensure the compliance of feed with requirements.

 (2) For the conduct of self-checking, a self-check plan in compliance with the requirements as laid down in Article 6 (2), Article 7 and Annex II to Regulation (EC) No 183/2005 of the European Parliament and of the Council shall be prepared in an undertaking.

 (3) The self-check plan and applied measures for ensuring the compliance of feed and the handling thereof with requirements form a system of self-checking. The data of a system of self-checking shall be documented and preserved for at least eighteen months.

§ 8.  [Repealed - RT I 2010, 72, 542 – entry into force 15.10.2010]

§ 9.  Handling and use of feed additives

  Feed additives and the premixtures including feed additives may be handled or used to feed animals in compliance with the requirements as laid down in Regulation (EC) No 1831/2003 of the European Parliament and of the Council.

§ 10.  [Repealed - RT I 2010, 72, 542 – entry into force 15.10.2010]

§ 11.  Use of feed intended for particular nutritional purposes

  The minister responsible for the area shall establish a list of purposes for feed intended for particular nutritional purposes and of methods needed for fulfilling such purposes.
[RT I 2010, 72, 542 – entry into force 15.10.2010]

§ 12.  [Repealed - RT I 2010, 72, 542 – entry into force 15.10.2010]

§ 13.  Handling and use of medicated feed

 (1) Medicated feed may only be produced from those premixtures for medicated feed which have been registered at the State Agency of Medicines as veterinary medicinal products and on the basis of prescriptions for medicated feed issued by veterinarians.

 (2) For the purposes of this Act, premixture for medicated feed means the premixture for medicated feed specified in subsection 6 (2) of the Medicinal Products Act.

 (3) Medicated feed shall conform to the corresponding prescription and shall be fed to animals according to the instructions by veterinarians without any additional processing.

 (4) The requirements for handling medicated feed shall be established by the minister responsible for the area.

§ 14.  Handling and use of genetically modified feed

 (1) Genetically modified feed and genetically modified organisms used in feed may be placed on the market in compliance with the requirements as laid down in Regulation (EC) No 1829/2003 of the European Parliament and of the Council.

 (11) For the purposes of Article 17 (2) of Regulation (EC) No 1829/2003 of the European Parliament and of the Council, a competent authority shall be the Veterinary and Food Board.
[RT I 2010, 72, 542 – entry into force 15.10.2010]

 (12) [Repealed - RT I, 10.11.2017, 2 - entry into force 01.01.2018]

 (2) [Repealed - RT I, 10.11.2017, 2 - entry into force 01.01.2018]

§ 15.  Use of feed for research

 (1) With the written consent of the Veterinary and Food Board, a research and development institution may convey feed additives which have not been entered in the register of feed additives of the Community as laid down in Article 17 of Regulation (EC) No 1831/2003 of the European Parliament and of the Council to Estonia and use the feed additives for research, including the making of tests, taking into account of the requirements as laid down in Article 3 (2) of Regulation (EC) No 1831/2003 of the European Parliament and of the Council.
[RT I 2010, 72, 542 – entry into force 15.10.2010]

 (2) The Veterinary and Food Board shall refuse to grant the consent specified in subsection (1) of this section if the research and development institution is unable to comply with the requirements as laid down in Article 3 (2) of Regulation (EC) No 1831/2003 of the European Parliament and of the Council or to ensure the harmlessness of feed.

 (3) The requirements on the content and format of the application submitted for the receipt of a written consent for the conveyance to Estonia and use for research of feed specified in subsection (1) of this section and the procedure for processing the application shall be established by the minister responsible for the area.

§ 16.  Conveyance of feed from third countries to Estonia

 (1) For the purposes of this Act, conveyance of feed to Estonia from a state or territory remaining outside of the customs territory of the European Union (hereinafter third country) means the activity as laid down in Article 3 (40) of Regulation (EU) 2017/625 of the European Parliament and of the Council.
[RT I, 04.12.2019, 2 – entry into force 14.12.2019]

 (11) Feed may be conveyed to Estonia from a third country through border crossing points open for international traffic based on the State Borders Act.
[RT I, 04.12.2019, 2 – entry into force 14.12.2019]

 (2) Feed specified in the list established under Article 47 (2) a) of Regulation (EU) 2017/625 of the European Parliament and of the Council may be conveyed from third countries to Estonia on the bases of and pursuant to the procedure as laid down in the Trade, Import and Export of Animals and Animal Products Act.
[RT I, 04.12.2019, 2 – entry into force 14.12.2019]

 (3) [Repealed - RT I 2010, 72, 542 – entry into force 15.10.2010]

 (4) [Repealed - RT I 2010, 72, 542 – entry into force 15.10.2010]

 (5) If, upon conveyance of feed unspecified in the list referred to in subsection (2) of this section (hereinafter non-animal feed) from a third country to Estonia, the compliance of feed must be inspected at a border crossing point or at the place of exercising official control over imported non-animal feed pursuant to the relevant legislation of the European Union, such feed may be conveyed to Estonia from a third country only through a border crossing point designated by the Veterinary and Food Board or through the place of exercising official control and the Veterinary and Food Board shall be notified of the conveyance of such feed to Estonia from a third country at least twenty-four hours before the submission of feed for exercising official control.
[RT I, 04.12.2019, 2 – entry into force 14.12.2019]

 (6) [Repealed - RT I, 04.12.2019, 2 – entry into force 14.12.2019]

 (7) [Repealed - RT I, 04.12.2019, 2 – entry into force 14.12.2019]

 (8) [Repealed - RT I, 04.12.2019, 2 – entry into force 14.12.2019]

 (9) [Repealed - RT I, 04.12.2019, 2 – entry into force 14.12.2019]

 (10) [Repealed - RT I, 04.12.2019, 2 – entry into force 14.12.2019]

§ 161.  Border inspection posts and places of exercising official control over imported non-animal feed

  [Repealed - RT I, 04.12.2019, 2 – entry into force 14.12.2019]

§ 162.  Border crossing point

 (1) Based on the application of the owner or possessor of a border crossing point open for international traffic pursuant to the State Borders Act, the Veterinary and Food Board shall designate the border crossing point through which non-animal feed may be conveyed to Estonia from a third country (hereinafter border crossing point) if a Member State has the right to designate a border crossing point according to the relevant legislation of the European Union.

 (2) The list of border crossing points shall be published on the website of the Veterinary and Food Board according to the requirements provided for in Article 60 of Regulation (EU) 2017/625 of the European Parliament and of the Council.

 (3) The Veterinary and Food Board shall submit to the European Commission a notice of the intention to designate a border crossing point in compliance with Article 59 (2) of Regulation (EU) 2017/625 of the European Parliament and of the Council.

 (4) After receipt of a notice from the European Commission provided for in Article 59 (3)–(5) of Regulation (EU) 2017/625 of the European Parliament and of the Council, the Veterinary and Food Board shall promptly make a relevant decision.

 (5) In the case provided for in Article 62 (1) and Article 63 (1) and (4) of Regulation (EU) 2017/60 of the European Parliament and of the Council, the Veterinary and Food Board shall make the relevant decision and an amendment in the list of border crossing points and notify the European Commission and other Member States thereof according to Articles 62 and 63 of the Regulation.

 (6) The requirements for the content of an application for designating a border crossing point specified in subsection (1) of this section and the procedure for processing the application shall be established by a regulation of the minister responsible for the area.
[RT I, 04.12.2019, 2 – entry into force 14.12.2019]

§ 163.  Place of exercising official control over imported non-animal feed

 (1) The Veterinary and Food Board shall, upon the request of a person, designate the place of exercising official control over imported non-animal feed if a Member State has the right to designate thereof according to the relevant legislation of the European Union. The place of exercising official control shall be in a place accepted by the Tax and Customs Board.

 (2) The list of places of exercising official control over imported non-animal feed shall be published on the website of the Veterinary and Food Board according to the requirements provided for in Article 53 (2) of Regulation (EU) 2017/625 of the European Parliament and of the Council.

 (3) If the place of exercising official control complies with the requirements referred to in Article 53 (1) a) of Regulation (EU) 2017/625 of the European Parliament and of the Council, The Veterinary and Food Board shall make a decision to designate a place of exercising official control over imported non-animal feed.

 (4) If the place of exercising official control does not comply with the requirements referred to in Article 53 (1) a) of Regulation (EU) 2017/625 of the European Parliament and of the Council, the Veterinary and Food Board shall make a decision to refuse to designate the place of exercising official control over imported non-animal feed.

 (5) The Veterinary and Food Board shall make a decision specified in subsection (3) or (4) of this section within 30 working days after receipt of an application for designating a place of exercising official control over imported non-animal feed.

 (6) In the case provided for in Article 62 (1) and Article 63 (1) and (4) of Regulation (EU) 2017/60 of the European Parliament and of Council and taking account of Article 53 (2), the Veterinary and Food Board shall make the relevant decision and an amendment in the list of places of exercising official control over imported non-animal feed and notify the European Commission and other Member States thereof according to Articles 62 and 63 of the Regulation.

 (7) The requirements for the content of an application for designating a place of exercising official control over imported non-animal feed specified in subsection (1) of this section and the procedure for processing the application shall be established by a regulation of the minister responsible for the area.
[RT I, 04.12.2019, 2 – entry into force 14.12.2019]

§ 17.  Export of feed

 (1) Feed can be exported in compliance with the requirements as laid down in Article 12 of Regulation (EC) No 178/2002 of the European Parliament and of the Council.
[RT I 2010, 72, 542 – entry into force 15.10.2010]

 (2) Upon the export of feed, the Veterinary and Food Board shall issue a document certifying the compliance of feed with requirements if the submission of such document is required in a third country.
[RT I 2010, 72, 542 – entry into force 15.10.2010]

Chapter 4 NOTIFICATION AND LICENCE OBLIGATION  
[RT I, 25.03.2011, 1 - entry into force 01.07.2014 (entry into force changed - RT I, 22.12.2013, 1)]

§ 18.  Notification obligation

 (1) A notice of economic activities shall be submitted to the Veterinary and Food Board in order to engage in the area of activity as laid down in Article 9 (2) a) of Regulation (EC) No 183/2005 of the European Parliament and of the Council.
[RT I, 29.06.2014, 1 – entry into force 01.07.2014]

 (2) The minister responsible for the area shall establish the specified list of the areas of activity and the substances used upon handling in the case of which a feed business operator is required to submit a notice of economic activities.
[RT I, 25.03.2011, 1 – entry into force 01.07.2014 (entry into force changed - RT I, 22.12.2013, 1)]

 (3) An undertaking shall not be required to pay state fee for entry of the data contained in the notice of economic activities specified in subsection (1) of this section in the national register of food and feed business operators.
[RT I, 29.06.2014, 1 – entry into force 01.07.2014]

§ 19.  Licence obligation

 (1) A feed business operator must hold an activity licence in the case as laid down in Article 10 of Regulation (EC) No 183/2005 of the European Parliament and of the Council or an activity licence for the manufacture of medicated feed.
[RT I, 29.06.2014, 1 – entry into force 01.07.2014]

 (2) An activity licence grants the feed business operator the right to commence and perform economic activities only in the undertaking or part of undertaking as specified in the activity licence.

 (3) The minister responsible for the area shall establish the specified list of the areas of activity and the substances used upon handling in the case of which a feed business operator is required to hold an activity licence.
[RT I, 25.03.2011, 1 – entry into force 01.07.2014 (entry into force changed - RT I, 22.12.2013, 1)]

§ 20.  Application for activity licence

 (1) An application for an activity licence shall be adjudicated by the Veterinary and Food Board by granting of or refusal to grant an activity licence within ninety days after the submission of an application for an activity licence.

 (2) In addition to the data specified in the General Part of the Economic Activities Code Act, an application for an activity licence shall include the self-check plan specified in subsection 7 (2) of this Act and the following documents contained therein depending on the nature of activities:
 1) documents certifying compliance with the principles of Hazard Analysis and Critical Control Point System (hereinafter HACCP);
 2) documents certifying the suitability of the structures and instruments for the intended purpose;
 3) cleaning and disinfection plan which includes data on the measures applied and substances used for the cleaning and disinfection of equipment and facilities;
 4) pest control plan which includes data on the measures applied for pest control;
 5) technological plan of the handling process with the significant parameters in view of feed safety and short description of the technology.

 (3) The Veterinary and Food Board shall send the list of undertakings who have been granted an activity licence and the data on the alteration of activity licences to the European Commission.

 (4) An undertaking shall not be required to pay state fee upon the adjudication of an application for an activity licence.
[RT I, 25.03.2011, 1 – entry into force 01.07.2014 (entry into force changed - RT I, 22.12.2013, 1)]

§ 201.  Subject of review of activity licence

  A feed business operator shall be granted an activity licence if his or her undertaking complies with the requirements of the legislation of the European Union and the requirements arising from this Act.
[RT I, 25.03.2011, 1 – entry into force 01.07.2014 (entry into force changed - RT I, 22.12.2013, 1)]

§ 21.  Specifications for suspension and prohibition of economic activities and suspension and revocation of activity licences

 (1) The Veterinary and Food Board shall suspend the economic activities of a feed business operator or revoke an activity licence partially or in full in the cases as laid down in Article 14 of Regulation (EC) No 183/2005 of the European Parliament and of the Council.

 (2) The Veterinary and Food Board shall prohibit the economic activities of an undertaking or revoke an activity licence partially or in full in the cases as laid down in Article 15 of Regulation (EC) No 183/2005 of the European Parliament and of the Council.
[RT I, 25.03.2011, 1 – entry into force 01.07.2014 (entry into force changed - RT I, 22.12.2013, 1)]

§ 22.  Revocation of approval decision and registration

  [Repealed - RT I, 25.03.2011, 1 – entry into force 01.07.2014 (entry into force changed - RT I, 22.12.2013, 1)]

§ 221.  Obligation to submit data on handling of feed

  A feed business operator who engages in the handling of feed shall submit to the Veterinary and Food Board, by the tenth date of the first month of each quarter, the following data for the preceding quarter concerning his or her undertaking which engages in the manufacture or processing of feed in the case of which the requirements as laid down in Article 5 (2) of Regulation (EC) No 183/2005 of the European Parliament and of the Council shall be followed:
 1) the type and quantity of feed manufactured and put into circulation;
 2) the quantity of feed materials manufactured and put into circulation;
 3) the quantity of compound feed manufactured and used for the production of animal products for putting into circulation.
[RT I, 25.03.2011, 1 – entry into force 01.07.2014 (entry into force changed - RT I, 22.12.2013, 1)]

Chapter 5 NATIONAL REGISTER OF FOOD AND FEED BUSINESS OPERATORS  
[RT I, 25.03.2011, 1 - entry into force 01.07.2014 (entry into force changed - RT I, 22.12.2013, 1)]

§ 23.  National register of food and feed business operators

  [RT I, 25.03.2011, 1 – entry into force 01.07.2014 (entry into force changed - RT I, 22.12.2013, 1)]

 (1) The aim of the national register of food and feed business operators (hereinafter the register) is to maintain records on the following to ensure an efficient official control:
 1) on food and feed business operators holding an activity licence;
 2) on food and feed business operators who have submitted a notice of economic activities for the handling of food or feed;
 3) on undertakings who have submitted a notice of economic activities for manufacturing, processing and putting into circulation of materials and items that come into contact with food.
[RT I, 13.03.2019, 2 – entry into force 15.03.2019]

 (11) The information specified in subsection 51 (1) of the General Part of the Economic Activities Code Act shall be entered in the register concerning a person and the activities thereof.
[RT I, 13.03.2019, 2 – entry into force 15.03.2019]

 (12) The register shall be founded and the statutes thereof shall be established by a regulation of the minister responsible for the area.
[RT I, 13.03.2019, 2 – entry into force 15.03.2019]

 (2) The controller of the register is the Ministry of Rural Affairs and the processor of the register shall be determined in the statutes of the register.
[RT I, 13.03.2019, 2 – entry into force 15.03.2019]

 (3) The submitter of the data is responsible for the correctness of such data. If data entered in the register change, an application for changing data shall be submitted immediately.

 (4) Registry data shall be public except for the data in the case of which a restriction on access has been established. State fee shall be paid for making an officially certified extract of registry data pursuant to the rate specified in the State Fees Act.

 (5) The provisions of the General Part of the Economic Activities Code Act concerning registers shall be applied to the register, taking account of the specifications provided for in this Act.
[RT I, 25.03.2011, 1 – entry into force 01.07.2014 (entry into force changed - RT I, 22.12.2013, 1)]

Chapter 6 OFFICIAL CONTROL AND OTHER OFFICIAL ACTIVITIES 
[RT I, 04.12.2019, 2 - entry into force 14.12.2019]

§ 24.  Performance of official control and other official activities

  [RT I, 04.12.2019, 2 – entry into force 14.12.2019]
The Veterinary and Food Board performs official control over compliance with the requirements established with the relevant legislation of the European Union, this Act and with the legislation established on the basis thereof on feed, handling of feed and feeding and performs other relevant official activities.
[RT I, 04.12.2019, 2 – entry into force 14.12.2019]

§ 25.  Authorised veterinarian

  [Repealed - RT I, 04.12.2019, 2 – entry into force 14.12.2019]

§ 26.  Special state supervision measures

  [RT I, 13.03.2014, 4 – entry into force 01.07.2014]
For the execution of state supervision provided for in this Act, the law enforcement agency may apply the special state supervision measures provided for in §§ 30, 31, 32, 49, 50 and 51 of the Law Enforcement Act on the basis of and pursuant to the procedure provided for in the Law Enforcement Act.
[RT I, 13.03.2014, 4 – entry into force 01.07.2014]

§ 261.  Specifications for state supervision

 (1) A business secret may be disclosed if maintaining it would endanger human or animal health or the environment. The following data are not deemed to be information subject to business secrecy:
 1) name and composition of the feed;
 2) physicochemical and biological characteristics of feed;
 3) pharmacological and toxicological characteristics of feed, and their effect on the environment;
 4) methods of analysis.

 (2) If a dwelling is also used as business premises, the law enforcement agency may examine it within office or opening hours without the permission of the administrative court specified in subsection 51 (2) of the Law Enforcement Act.
[RT I, 13.03.2014, 4 – entry into force 01.07.2014]

§ 27.  Precept

  [Repealed - RT I, 25.03.2011, 1 – entry into force 01.07.2014 (entry into force changed - RT I, 22.12.2013, 1)]

§ 28.  Organisation of official control

  [RT I, 13.03.2014, 4 – entry into force 01.07.2014]

 (1) Official control over feed, handling of feed and feeding shall be organised pursuant to the control plan prepared on the basis of Article 109 of Regulation (EU) 2017/60 of the European Parliament and of Council. The control plan shall be published on the website of the Veterinary and Food Board according to Article 111 of the aforesaid Regulation.
[RT I, 04.12.2019, 2 – entry into force 14.12.2019]

 (2) The data concerning the results of official control provided for in Article 11 (1) of Regulation (EU) 2017/60 of the European Parliament and of the Council shall be published on the website of the Veterinary and Food Board.
[RT I, 04.12.2019, 2 – entry into force 14.12.2019]

 (3) [Repealed - RT I, 04.12.2019, 2 – entry into force 14.12.2019]

 (4) The tariff classification of the feed upon release for free circulation of which state fee shall be paid for official control operations according to the rates specified in subsection 252 (3) of the State Fees Act shall be established by the minister responsible for the area.
[RT I, 30.12.2014, 1 – entry into force 01.01.2015]

 (5) The Veterinary and Food Board shall be the liasion body for the purposes of Article 103 (1) of Regulation (EU) 2017/60 of the European Parliament and of Council.
[RT I, 04.12.2019, 2 – entry into force 14.12.2019]

 (6) A feed business operator shall pay state fee for exercising official control, including supervisory activities for every undertaking which engages in the activity as laid down in Article 5 (2) of Regulation (EC) No 183/2005 of the European Parliament and of the Council pursuant to the rate specified in the State Fees Act. State fee shall not be paid for an undertaking which engages in the sale of packaged feed in retail business.
[RT I, 13.03.2014, 4 – entry into force 01.07.2014]

 (7) The Veterinary and Food Board shall be the authority who coordinates the preparation of the contingency plan specified in Article 115 of Regulation (EU) 2017/60 of the European Parliament and of the Council and the authority responsible for the multi-annual national control plan specified in Article 109 (2). The Veterinary and Food Board shall submit the multi-annual national control plan and the implementation report thereof to the European Commission according to Article 113 of the aforesaid Regulation.
[RT I, 04.12.2019, 2 – entry into force 14.12.2019]

 (8) The Government of the Republic may establish by a regulation the procedure of cooperation between law enforcement agencies for the preparation of the contingency plan and multi-annual national control plan specified in subsection (7) of this section.
[RT I, 04.12.2019, 2 – entry into force 14.12.2019]

 (9) Other law enforcement agency, administrative body or governmental authority shall promptly notify the Veterinary and Food Board in case of the following potential violation of requirements concerning feed, handling of feed and feeding:
 1) a violation that may pose a serious risk to animal or human health, animal’s wellbeing or to the environment;
 2) a violation that has been committed by knowingly creating an incorrect image of the actual circumstances.
[RT I, 04.12.2019, 2 – entry into force 14.12.2019]

§ 29.  Measures taken upon detection of non-conforming feed

 (1) Upon detection of non-conforming feed, the Veterinary and Food Board shall take the measures as laid down in Article 138 of Regulation (EU) 2017/60 of the European Parliament and of the Council.
[RT I, 04.12.2019, 2 – entry into force 14.12.2019]

 (2) Upon conveyance of non-conforming feed from third countries to Estonia, the Veterinary and Food Board shall take the measures as laid down in Article 66 of Regulation (EU) 2017/60 of the European Parliament and of the Council.
[RT I, 04.12.2019, 2 – entry into force 14.12.2019]

 (3) Feed subject to destruction shall be treated in compliance with the requirements specified in the Waste Act.

 (4) The measures specified in subsections (1) and (2) of this section shall be applied at the expense of the feed business operator and in a manner which does not endanger human and animal health or the environment.

 (5) The Veterinary and Food Board shall notify the European Commission of harmful feed in terms of food safety through the rapid alert system as laid down in Article 50 of Regulation (EC) No 178/2002 of the European Parliament and of the Council.

Chapter 61 TAKING OF AND ANALYSIS OF SAMPLES AND LABORATORIES  
[RT I, 13.03.2014, 4 - entry into force 01.07.2014]

§ 30.  Taking of samples upon performing official control or other official activities

  [RT I, 04.12.2019, 2 – entry into force 14.12.2019]

 (1) Upon performing official control or other official activities, samples may be taken at the expense of a person upon the examination of a movable. If the examined movable cannot be used as normal after the examination, the cost of the movable or the cost of restoration of the movable for normal use shall not be reimbursed to the person.
[RT I, 04.12.2019, 2 – entry into force 14.12.2019]

 (2) The procedure for taking of feed samples during official control or other official activities shall be established by the minister responsible for the area.
[RT I, 04.12.2019, 2 – entry into force 14.12.2019]

 (3) A batch of feed from which a sample has been taken during official control or other official activities may be used or transferred only after receipt of a corresponding permission from the Veterinary and Food Board.
[RT I, 04.12.2019, 2 – entry into force 14.12.2019]

 (4) A feed business operator may request that in addition to the sample specified in subsection (1) of this section, an additional sample is taken at the expense of the operator on the same conditions and which shall remain at his or her disposal.
[RT I, 04.12.2019, 2 – entry into force 14.12.2019]

§ 31.  Analysis of samples

 (1) [Repealed - RT I, 04.12.2019, 2 – entry into force 14.12.2019]

 (2) [Repealed - RT I 2009, 48, 321 – entry into force 23.10.2009]

 (3) Samples taken during official controls and other official activities shall be analysed in an official laboratory authorised by the Veterinary and Food Board for performing relevant analyses (hereinafter official laboratory) which complies with the requirements as laid down in Article 37 (4) and (5) of Regulation (EU) 2017/60 of the European Parliament and of the Council.
[RT I, 04.12.2019, 2 – entry into force 14.12.2019]

 (31) A non-accredited laboratory may also be authorised to act as an official laboratory in the cases provided for in Articles 40 and 42 of Regulation (EU) 2017/60 of the European Parliament and of the Council.
[RT I, 04.12.2019, 2 – entry into force 14.12.2019]

 (4) Information on the laboratories in which samples taken in the course of official control are analysed shall be published on the website of the Veterinary and Food Board.
[RT I, 13.03.2014, 4 – entry into force 01.07.2014]

 (5) In case of a dispute between the Veterinary and Food Board and a feed business operator arising from a second expert opinion provided for in Article 35 of Regulation (EU) 2017/60 of the European Parliament and of the Council, the operator may request, at his or her own expense, the documentary review of the initial analysis and, where appropriate, another analysis of the sample specified in subsection 30 (4) of this Act by another laboratory specified in Article 37 (1) of the aforesaid Regulation.
[RT I, 04.12.2019, 2 – entry into force 14.12.2019]

 (6) Regardless of requesting a second expert opinion, the Veterinary and Food Board shall apply the necessary measures provided for in Article 66 or 138 of Regulation (EU) 2017/60 of the European Parliament and of the Council.
[RT I, 04.12.2019, 2 – entry into force 14.12.2019]

 (7) The expenses of analysing samples taken in the course of official control shall be covered from the state budget.
[RT I, 13.03.2014, 4 – entry into force 01.07.2014]

 (8) [Repealed - RT I, 13.03.2014, 4 – entry into force 01.07.2014]

§ 32.  Reference laboratory

 (1) National reference laboratory (hereinafter reference laboratory) shall be authorised for each European Union reference laboratory on feed as laid down in Article 93 (1) of Regulation (EU) 2017/60 of the European Parliament and of the Council. Laboratory complying with the requirements specified in Article 100 (2) and (3) of Regulation (EU) 2017/60 of the European Parliament and of the Council can be authorised as reference laboratory.
[RT I, 04.12.2019, 2 – entry into force 14.12.2019]

 (2) Authorisation to operate as a reference laboratory shall be granted to a laboratory by a directive of the minister responsible for the area, which shall set out the scope of the authorisation.

 (3) The procedure for applying for and grant of the authorisation to operate as a reference laboratory shall be established by a regulation of the minister responsible for the area.
[RT I, 04.12.2019, 2 – entry into force 14.12.2019]

 (4) If a reference laboratory fails to perform its functions as required or does not comply with the requirements specified in subsection 31 (3) of this Act, the minister responsible for the area shall specify a term for the elimination of deficiencies and may suspend the validity of the directive specified in subsection (2) of this section partially or in full.

 (5) If the deficiencies are not eliminated within the specified term, the minister responsible for the area shall revoke the directive specified in subsection (2) of this section partially or in full.

Chapter 7 LIABILITY 

§ 33.  Violation of requirements for feed

 (1) Violation of the requirements for feed in a manner which endangers human or animal health or the environment is punishable by a fine of up to 300 fine units.

 (2) The same act, if committed by a legal person, is punishable by a fine of up to 3,200 euros.
[RT I 2010, 22, 108 – entry into force 01.01.2011]

§ 34.  Violation of requirements for labelling of feed

 (1) Violation of the requirements for the labelling of feed, or adulteration of feed is punishable by a fine of up to 300 fine units.

 (2) The same act, if committed by a legal person, is punishable by a fine of up to 3,200 euros.
[RT I 2010, 22, 108 – entry into force 01.01.2011]

§ 35.  Violation of requirements for handling of feed and feeding to animals

 (1) Violation of the requirements for the handling of feed or feeding to animals, including failure to comply with the recording requirement is punishable by a fine of up to 300 fine units.

 (2) The same act, if committed by a legal person, is punishable by a fine of up to 3,200 euros.
[RT I 2010, 22, 108 – entry into force 01.01.2011]

§ 36.  Failure to notify of conveyance of feed from third countries to Estonia

 (1) Failure to notify the Veterinary and Food Board of conveyance of feed from third countries to Estonia, if notification is required under this Act, is punishable by a fine of up to 150 fine units.

 (2) The same act, if committed by a legal person, is punishable by a fine of up to 640 euros.
[RT I 2010, 22, 108 – entry into force 01.01.2011]

§ 361.  Violation of notification obligation

 (1) Violation of the requirement for notification obligation specified in § 18 of this Act is punishable by a fine of up to 150 fine units.

 (2) The same act, if committed by a legal person, is punishable by a fine of up to 640 euros.
[RT I, 25.03.2011, 1 – entry into force 01.07.2014 (entry into force changed - RT I, 22.12.2013, 1)]

§ 37.  Failure to notify of quantity of feed

  [Repealed - RT I, 04.12.2019, 2 – entry into force 14.12.2019]

§ 38.  Proceedings

 (1) The Veterinary and Food Board is the extra-judicial body which conducts proceedings in matters of misdemeanours provided for in this chapter.

 (2) A court or the extra-judicial body which conducts proceedings in matters of misdemeanours specified in subsection (1) of this section may, pursuant to § 83 of the Penal Code, apply confiscation of the substance or product which was the direct object of the commission of a misdemeanour provided for in § 33 of this Act.
[RT I, 12.07.2014, 1 – entry into force 01.01.2015]

Chapter 8 IMPLEMENTING PROVISIONS  

§ 39.  Repeal of Feedingstuffs Act

  The Feedingstuffs Act (RT I 2002, 18, 97; 2006, 21, 162) is repealed.

§ 40.  Reorganisation of state supervision

 (1) [Repealed - RT I 2009, 48, 321 – entry into force 23.10.2009]

 (2) [Repealed - RT I 2009, 48, 321 – entry into force 23.10.2009]

 (3) [Repealed - RT I 2009, 48, 321 – entry into force 23.10.2009]

 (4) Upon exercising state supervision over compliance with the requirements specified in §§ 13 and 15 of this Act, the supervisory officials of the Veterinary and Food Board perform the functions of supervisory officials provided for in this Act and they shall have all the rights of supervisory officials as of entry into force of this Act.

 (5) [Repealed - RT I 2009, 48, 321 – entry into force 23.10.2009]

 (6) [Repealed - RT I 2009, 48, 321 – entry into force 23.10.2009]

 (7) [Repealed - RT I 2009, 48, 321 – entry into force 23.10.2009]

§ 41.  [Repealed - RT I 2009, 48, 321 – entry into force 23.10.2009]

§ 42.  Other transitional provisions

 (1) Undertakings approved or registered on the basis of subsection 23 (4) of the previous Feedingstuffs Act may continue its activity until the revocation or amendment of the approval or registration decision made on the basis of the previous Feedingstuffs Act.

 (2) [Repealed - RT I 2009, 48, 321 – entry into force 23.10.2009]

 (3) The State Register of Feedingstuffs founded on the basis of § 28 of the previous Feedingstuffs Act shall be deemed to be the State Register of Feedingstuffs specified in § 23 of this Act.

 (4) [Repealed - RT I 2009, 48, 321 – entry into force 23.10.2009]

 (5) [Repealed - RT I 2009, 48, 321 – entry into force 23.10.2009]

§ 421.  Border inspection posts and places of exercising supervision entered in the list of border inspection posts and places of exercising supervision over imported non-animal feed before 15 October 2010

  Border inspection posts and places of exercising supervision entered in the list of border inspection posts and places of exercising supervision over imported non-animal feed on the website of the Veterinary and Food Board before 15 October 2010 shall remain in the given list until the Veterinary and Food Board makes a decision on the exclusion of the border inspection post or place of exercising supervision from the given list.
[RT I 2010, 72, 542 – entry into force 15.10.2010]

§ 422.  Places of exercising official control

  The places of exercising supervision entered in the list of border inspection posts and places of exercising supervision over imported feed shall be deemed to be the places of exercising official control.
[RT I, 29.06.2014, 2 – entry into force 01.07.2014]

§ 423.  National register of food and feed business operators

  The national register of food and feed business operators founded on the basis of subsection 23 (1) of this Act in the wording in force on 1 July 2014 shall be deemed to be the national register of food and feed business operators specified in § 23 of this Act.
[RT I, 13.03.2019, 2 – entry into force 15.03.2019]

§ 424.  Submission of data on handling feed

  A feed business operator, who in the last quarter of 2019, operates in an undertaking engaged in the manufacture or processing of feed in case of which the requirements provided for in Article 5 (2) of Regulation (EU) 2017/60 of the European Parliament and of the Council must be complied with, shall submit to the Veterinary and Food Board by 10 January 2020 the data on the last quarter of 2019:
 1) the type and quantity of feed manufactured and put into circulation;
 2) the quantity of feed materials manufactured and put into circulation;
 3) the quantity of compound feed manufactured and used for the production of animal products for putting into circulation.
[RT I, 04.12.2019, 2 – entry into force 14.12.2019]

§ 425.  Payment of state fee

 (1) A feed business operator shall pay by 10 January 2020 state fee for the performance of official control, including supervisory activities for every undertaking which, in the last quarter of 2019, engages in the activity as laid down in Article 5 (2) of Regulation (EC) No 183/2005 of the European Parliament and of the Council pursuant to the rate specified in the State Fees Act. State fee shall not be paid for an undertaking which engages in the sale of packaged feed in retail business.

 (2) Upon releasing feed for free circulation, state fee shall be paid by 10 January 2020 in case of feeds for which tariff classification has been established on the basis of subsection 28 (4) of the wording of this Act in force until 31 December 2019.
[RT I, 04.12.2019, 2 – entry into force 14.12.2019]

§ 43. – § 46. [Omitted from this text]

§ 47.  Entry into force of Act

 (1) This Act enters into force on 1 February 2007.

 (2) § 44 of this Act enters into force on 1 July 2007.


1Commission Directive 82/475/EEC laying down the categories of ingredients which may be used for the purposes of labelling compound feedingstuffs for pet animals (OJ L 213, 21.07.1982, p. 27–28), amended with Directives 91/334/EEC (OJ L 184, 10.07.1991, p. 27) and 98/67/EC (OJ L 261, 24.09.1998, p. 10–31); Council Directive 90/167/EEC laying down the conditions governing the preparation, placing on the market and use of medicated feedingstuffs in the Community (OJ L 92, 07.04.1990, p. 42–48); Directive 2002/32/EC of the European Parliament and of the Council on undesirable substances in animal feed (OJ L 140, 30.05.2002, p. 10–22), amended with Directives 2003/57/EC (OJ L 151, 19.06.2003, p. 38–41), 2003/100/EC (OJ L 285, 01.11.2003, p. 33–37), 2005/8/EC (OJ L 27, 29.01.2005, p. 44–45), 2005/86/EC (OJ L 318, 06.12.2005, p. 16–18), 2005/87/EC (OJ L 318, 06.12.2005, p. 19–24), 2006/13/EC (OJ L 32, 04.02.2006, p. 44–53), 2006/77/EC (OJ L 271, 30.09.2006, p. 53–55), 2008/76/EC (OJ L 198, 26.07.2008, p. 37–40), 2009/8/EC (OJ L 40, 11.02.2009, p. 19–25), 2009/124/EC (OJ L 254, 26.09.2009, p. 100–103), 2009/141/EC (OJ L 308, 24.11.2009, p. 20–23) and 2010/6/EU (OJ L 37, 10.02.2010, p. 29–32) and Regulations (EC) No 219/2009 (OJ L 87, 31.03.2009, p. 109–154), (EU) No 574/2011 (OJ L 159, 17.06.2011, p. 7–24), (EU) No 277/2012 (OJ L 91, 29.03.2012, p. 1–7), (EU) No 744/2012 (OJ L 219, 17.08.2012, p. 5–12), (EU) No 107/2013 (OJ L 35, 06.02.2013, p. 1–2), (EU) No 1275/2013 (OJ L 328, 07.12.2013, p. 86–92), (EU) 2015/186 (OJ L 31, 07.02.2015, p. 11–17), (EU) 2017/2229 (OJ L 319, 05.12.2017, p. 6–9) and (EU) 2019/1243 (OJ L 198, 25.07.2019, p. 241–344); Commission Directive 2003/7/EC amending the conditions for authorisation of canthaxanthin in feedingstuffs in accordance with Council Directive 70/524/EEC (OJ L 22, 25.01.2003, p. 28–30); Commission Directive 2008/38/EC establishing a list of intended uses of animal feedingstuffs for particular nutritional purposes (Codified version) (OJ L 62, 06.03.2008, p. 9–22), amended with Directive 2008/82/EC (OJ L 202, 31.07.2008, p. 48–49) and Regulations (EU) No 1070/2010 (OJ L 306, 23.11.2010, p. 42–43), (EU) No 5/2014 (OJ L 2, 07.01.2014, p. 3–9) and (EU) No 1123/2014 (OJ L 304, 23.10.2014, p. 81–86). [RT I, 04.12.2019, 2 – entry into force 14.12.2019]

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