Sec. 13.
A person manufacturing or distributing commercial feed shall comply with all of the following:
(a) The "AAFCO Model Good Manufacturing Practice Regulations for Feed and Feed Ingredients" as published within the AAFCO official publication, which is hereby incorporated by reference. These regulations apply in determining whether a commercial feed meets either of the following:
(i) Is adulterated within the meaning of section 8.
(ii) Has been produced, prepared, packed, or held under unsanitary conditions through which it may have become contaminated with filth or rendered unwholesome or unsafe to animal or public health.
(b) The requirements in 21 CFR 558.6 for a veterinary feed directive drug as defined in 21 CFR 558.3.
(c) The requirements in 21 CFR 589.1 to 589.2001 for prohibited mammalian protein.
(d) The following requirements of manufacturing or distributing commercial feeds containing drugs:
(i) The regulation prescribing good manufacturing practices for type B and type C medicated feeds in 21 CFR 225.1 to 225.202.
(ii) The regulations prescribing good manufacturing practices for type A medicated articles in 21 CFR 226.1 to 226.115.
History: 1975, Act 120, Imd. Eff. June 26, 1975 ;-- Am. 2015, Act 83, Eff. Oct. 1, 2015
Last modified: October 10, 2016