FDA Inspection 985003 - Woodbine Products Company - September 06, 2016

FDA Inspection 985003 for Woodbine Products Company on September 06, 2016. Classification: Voluntary Action Indicated (VAI).

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Record Summary

FDA Inspection 985003 for Woodbine Products Company on September 06, 2016. Classification: Voluntary Action Indicated (VAI).

Violation Codes

21 CFR 211.100(a)

21 CFR 211.160(b)

21 CFR 211.166(a)

21 CFR 211.192

21 CFR 211.22(a)

21 CFR 211.22(d)

21 CFR 211.84(a)

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Record Information

Company

Woodbine Products Company

Inspection Date

September 6, 2016

Product Type

Drugs

Office

Center for Drug Evaluation and Research

ID: fd85a7ba-c272-4184-817d-f4e3632e4afe

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