FDA Inspection 635530 - Acuity Specialty Products, Inc - December 18, 2009

FDA Inspection 635530 for Acuity Specialty Products, Inc on December 18, 2009. Classification: Voluntary Action Indicated (VAI).

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Record Summary

FDA Inspection 635530 for Acuity Specialty Products, Inc on December 18, 2009. Classification: Voluntary Action Indicated (VAI).

Violation Codes

21 CFR 211.110(a)

21 CFR 211.137(a)

21 CFR 211.166(a)

21 CFR 211.84(d)(2)

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Record Information

Company

Acuity Specialty Products, Inc

Inspection Date

December 18, 2009

Product Type

Drugs

Office

Center for Drug Evaluation and Research

ID: 9be3601d-5db5-44a0-a4d0-6f2fff44c832

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