FDA Inspection 744219 - Fareva Amboise - September 20, 2011

FDA Inspection 744219 for Fareva Amboise on September 20, 2011. Classification: Voluntary Action Indicated (VAI).

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Record Summary

FDA Inspection 744219 for Fareva Amboise on September 20, 2011. Classification: Voluntary Action Indicated (VAI).

Violation Codes

21 CFR 211.110(a)

21 CFR 211.110(b)

21 CFR 211.165(f)

21 CFR 211.192

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Record Information

Company

Fareva Amboise

Inspection Date

September 20, 2011

Product Type

Drugs

Office

Center for Drug Evaluation and Research

ID: fa7cbbfc-49aa-4fd1-976c-fbb53a828a47

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