§ 111.120. What quality control operations are required for components, packaging, and labels before use in the manufacture of a dietary supplement?
102 words·~1 min read·
/us/cfr/t21/s§ 111.120·A research copy — for the controlling text, always check the official state or federal source. Not legal advice.
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.