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.
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