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A COA that includes particulate matter testing (USP ) documents that the product has been evaluated for this class of contamination

[DOI] [PMC free article] [PubMed] [Google Scholar] Cao Y

The FDA concluded that the company's manufacturing systems, laboratory controls, and quality oversight failed to comply with Current Good Manufacturing Practice (CGMP) requirements, ultimately classifying products manufactured at the facility as adulterated under the Federal Food, Drug, and Cosmetic Actnot because contamination was confirmed, but because the quality systems could no longer be relied upon

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