21 CFR § 111.525 Current Good Manufacturing Practice in Manufacturing, Packaging, Labeling, or Holding Operations for Dietary Supplements

§ 111.525 What requirements apply to a returned dietary supplement that quality control personnel approve for reprocessing?

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

(a) You must ensure that any returned dietary supplements that are reprocessed meet all product specifications established in accordance with § 111.70(e); and

(b) Quality control personnel must approve or reject the release for distribution of any returned dietary supplement that is reprocessed.

← § 111.520 When may a returned dietary supplement be salvaged?§ 111.530 When must an investigation be conducted of your manufacturing processes and other batches? →