Quality control operations for components, packaging, and labels before use in the manufacture of a dietary supplement must include:

1. (a) Reviewing all receiving records for components, packaging, and labels;
2. (b) Determining whether all components, packaging, and labels conform to specifications established under § 111.70 (b) and (d);
3. (c) Conducting any required material review and making any required disposition decision;
4. (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
5. (e) Approving, and releasing from quarantine, all components, packaging, and labels before they are used.