Code of Federal Regulations Title 21. Food and Drugs § 21.111.120 What quality control operations are required for components, packaging, and labels before use in the manufacture of a dietary supplement?

(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.