StacksVerified U.S. regulatory reference

21 CFR §111.130

Verified against eCFR.gov as of June 20, 2026View official text on eCFR.gov ↗
Quality control operations for returned dietary supplements must include:
  1. (a)Conducting any required material review and making any required disposition decision; including:
    1. (1)Determining whether tests or examination are necessary to determine compliance with product specifications established in accordance with § 111.70(e); and
    2. (2)Reviewing the results of any tests or examinations that are conducted to determine compliance with product specifications established in accordance with § 111.70(e);
  2. (b)Approving or rejecting any salvage and redistribution of any returned dietary supplement;
  3. (c)Approving or rejecting any reprocessing of any returned dietary supplement; and
  4. (d)Determining whether the reprocessed dietary supplement meets product specifications and either approving for release, or rejecting, any returned dietary supplement that is reprocessed.