§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:
Reviewing all receiving records for components, packaging, and labels;
Determining whether all components, packaging, and labels conform to specifications established under § 111.70 (b) and (d);
Conducting any required material review and making any required disposition decision;
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
Approving, and releasing from quarantine, all components, packaging, and labels before they are used.
Notes, amendments, and revision history
Authority
Authority: 21 U.S.C. 321, 342, 343, 371, 374, 381, 393; 42 U.S.C. 264.
Source
Source: 72 FR 34942, June 25, 2007, unless otherwise noted.