Contents
1.The specific maximum levels of cross-contamination in non-target feed for the antimicrobial active substances listed in Annex II to Regulation (EU) 2019/4 shall be set:
(a)where the last batch manufactured, processed, stored or transported before the manufacturing, processing, storage or transport of the non-target feed is medicated feed, at 1 % of the antimicrobial active substance contained in that last batch of medicated feed, relative to a moisture content of 12 % in the non-target feed;
(b)where the last batch manufactured, processed, stored or transported before the manufacturing, processing, storage or transport of the non-target feed is an intermediate product, at 1 % of the antimicrobial active substance to be contained in the medicated feed derived from that last batch of intermediate product, relative to a moisture content of 12 % in the non-target feed.
Source: EUR-Lex, © European Union, 1998-2026. Reuse authorised under Decision 2011/833/EU.