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Code · CFR · Title 21 — Food and Drugs · Part 111 — Current Good Manufacturing Practice in Manufacturing, Packaging, Labeling, or Holding Operations for Dietary Supplements · § 111.370

§ 111.370. What requirements apply to rejected dietary supplements?

30 words·~1 min read·/us/cfr/t21/s§ 111.370·

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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.
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