';


Title 21 Part 111 → Subpart F → §111.120

Title 21 → Chapter I → Subchapter B → Part 111 → Subpart F → §111.120

Electronic Code of Federal Regulations e-CFR

Title 21 Part 111 → Subpart F → §111.120

§111.120   What quality control operations are required for components, packaging, and labels before use in the manufacture of a dietary supplement?

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.