21 CFR § 111.370 Current Good Manufacturing Practice in Manufacturing, Packaging, Labeling, or Holding Operations for Dietary Supplements

§ 111.370 What requirements apply to rejected dietary supplements?

Current through Sep 8, 2026 · Read all of Part 111

You must clearly identify, hold, and control under a quarantine system for appropriate disposition any dietary supplement that is rejected and unsuitable for use in manufacturing, packaging, or labeling operations.

← § 111.365 What precautions must you take to prevent contamination?§ 111.375 Under this subpart K, what records must you make and keep? →