§ 111.127. What quality control operations are required for packaging and labeling operations?
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/us/cfr/t21/s§ 111.127·A research copy — for the controlling text, always check the official state or federal source. Not legal advice.
Quality control operations for packaging and labeling operations must include:
(a)Reviewing the results of any visual examination and documentation to ensure that specifications established under § 111.70(f) are met for all products that you receive for packaging and labeling as a dietary supplement (and for distribution rather than for return to the supplier);
(b)Approving, and releasing from quarantine, all products that you receive for packaging or labeling as a dietary supplement (and for distribution rather than for return to the supplier) before they are used for packaging or labeling;
(c)Reviewing and approving all records for packaging and label operations;
(d)Determining whether the finished packaged and labeled dietary supplement conforms to specifications established in accordance with § 111.70(g);
(e)Conducting any required material review and making any required disposition decision;
(f)Approving or rejecting any repackaging of a packaged dietary supplement;
(g)Approving or rejecting any relabeling of a packaged and labeled dietary supplement; and
(h)Approving for release, or rejecting, any packaged and labeled dietary supplement (including a repackaged or relabeled dietary supplement) for distribution.