Code of Federal Regulations · Section
§ 111.120 — What Quality Control Operations Are Required For Components, Packaging, And Labels Before Use In The Manufacture Of A Dietary Supplement?
21 C.F.R. § 111.120
Quality control operations for components, packaging, and labels before use in the manufacture of a dietary supplement must include:
(a) Reviewing all receiving records for components, packaging, and labels;
(b) Determining whether all components, packaging, and labels conform to specifications established under § 111.70 (b) and (d);
(c) Conducting any required material review and making any required disposition decision;
(d) Approving or rejecting any treatment and in-process adjustments of components, packaging, or labels to make them suitable for use in the manufacture of a dietary supplement; and
(e) Approving, and releasing from quarantine, all components, packaging, and labels before they are used.
Authorizing Statute
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Regulations to control communicable diseases42 U.S.C. § 264
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Definitions; generally21 U.S.C. § 321