FDA Inspection 650331 - McKesson Corporation dba RxPak - March 01, 2010

FDA Inspection 650331 for McKesson Corporation dba RxPak on March 01, 2010. Classification: Voluntary Action Indicated (VAI).

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Record Summary

FDA Inspection 650331 for McKesson Corporation dba RxPak on March 01, 2010. Classification: Voluntary Action Indicated (VAI).

Violation Codes

21 CFR 211.115(b)

21 CFR 211.25(a)

21 CFR 211.68(b)

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Record Information

Company

McKesson Corporation dba RxPak

Inspection Date

March 1, 2010

Product Type

Drugs

Office

Center for Drug Evaluation and Research

ID: 0e09a648-088a-4e9e-a4e9-0e6dc10899b7

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