FDA Inspection 850250 - Avista Pharma Solutions, Inc. dba Cambrex - September 27, 2013

FDA Inspection 850250 for Avista Pharma Solutions, Inc. dba Cambrex on September 27, 2013. Classification: Voluntary Action Indicated (VAI).

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Record Summary

FDA Inspection 850250 for Avista Pharma Solutions, Inc. dba Cambrex on September 27, 2013. Classification: Voluntary Action Indicated (VAI).

Violation Codes

21 CFR 211.100(a)

21 CFR 211.113(b)

21 CFR 211.160(a)

21 CFR 211.165(a)

21 CFR 211.192

21 CFR 211.42(c)(10)

21 CFR 211.42(c)(10)(iv)

21 CFR 211.84(d)(2)

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Record Information

Company

Avista Pharma Solutions, Inc. dba Cambrex

Inspection Date

September 27, 2013

Product Type

Drugs

Office

Center for Drug Evaluation and Research

ID: 51fdbe29-4c8a-4db0-b664-5ef7edf67340

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