...control of the product. (An application may be refused unlass it includes adequate Information showing that the methods used in, and the facilities and controls used for, the manufacturing, proc.. esslng, and packaging of the drug are adequate to preserve Its identity, strength, quality,...

...control of the product. (An application may be refused unless it includes adequate information showing that the methods used in, and the facilities and controls used for, the manufacturing, processing, and packaging of the drug are adequate to preserve its identity, strength, quality and purity in conformity...

...control of the product. (An application may be refused unless it includes adequate information showing that the methods used in, and the facilities and controls used for, the manufacturing, processing, and packaging of the drug are adequate to preserve its identity, strength, quality and purity in conformity...

...omits or fails to conform to other applicable information published pursuant to subsection (i) : "(C) that the methods used in, and the facilities and controls used for, the manufacturing, processing, and packing of such animal feed are inadequate to preserve the identity, strength, quality, and purity...

...omits or fails to conform to other applicable information published pursuant to subsection (i) ; "(C) that the methods used in, and the facilities and controls used for. the manufacturing, processing, and packing of such animal feed are inadequate to preserve the identity, strength, quality, and purity...

...omits or fails to conform to other applicable information published pursuant to subsection (i) ; "(C) that the methods used in, and the facilities and controls used for, the manufacturing, processing, and packing of such animal feed are inadequate to preserve the identity, strength, quality, and purity...

...for introduction into interstate oramerce of articles of drugs which purport or are represented .. be sterile which are adulterated within the meaning...or holding of said articles do not conform to and are not operated and administered in conformity with Current .^ood Manufacturing Practice as prescribed...

...caused to be introduce 1 -rd delivered for introduction into interstate comerce, as aforesa: '., v;as adulterated within the meaning of 21 USC 351(a)(2)(B) in that the methods used in, and the; facilities and controls used for the manuf;.: ture, processing, packing and holding of said drug did not ccnfom...

...control of the product. (An application may be refused unless it includes adequate Information showing that the methods used in, and the facilities and controls used for, the manufacturing, processing, and packaging of the drug are adequate to preserve its Identity, strength, quality, and purity In conformity...

...control of the product. (An application may be refused unless it Includes adequate information showing that the methods used in, and the facilities and controls used for, the manufacturing, processing, and packaging of the drug are adequate to preserve its identity, strength, quality, and purity In conformity...