39-14-52. Adulteration by drug not conforming to good manufacturing practice.
A commercial feed shall be deemed to be adulterated if it contains a drug and the methods used in or the facilities or controls used for its manufacture, processing, or packaging do not conform to current good manufacturing practice rules promulgated by the secretary of agriculture and natural resources pursuant to the provisions of chapter 1-26 to assure that the drug meets the requirement of this chapter as to safety and has the identity and strength and meets the quality and purity characteristics which it purports or is represented to possess. In promulgating such rules, the secretary shall adopt the current good manufacturing practice regulations for medicated feed premixes and for medicated feeds established under authority of the Federal Food, Drug, and Cosmetic Act, unless he determines that they are not appropriate to the conditions which exist in this state.
Source: SL 1970, ch 228, §7 (4); SL 1986, ch 326, §71; SL 2021, ch 1 (Ex. Ord. 21-3), § 51, eff. Apr. 19, 2021.