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21 U.S.C. 321, 342, 343, 371, 374, 381, 393; 42 U.S.C. 264.
72 FR 34942, June 25, 2007, unless otherwise noted.
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You must use adequate laboratory facilities to perform whatever testing and examinations are necessary to determine whether:
(a) Components that you use meet specifications;
(b) In-process specifications are met as specified in the master manufacturing record; and
(c) Dietary supplements that you manufacture meet specifications.