Violations Of 21 CFR Part 820 Quality System Regulation, Subparts H-I: Acceptance Activities and Nonconforming Product: Warning Letters Issued by U.S. ... Administration (FDA Warning Letters Analysis)
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Violations Of 21 CFR Part 820 Quality System Regulation, Subparts H-I: Acceptance Activities and Nonconforming Product: Warning Letters Issued by U.S. ... Administration (FDA Warning Letters Analysis)
