FDA Inspection 703101 - Unither Manufacturing LLC. - November 23, 2010

FDA Inspection 703101 for Unither Manufacturing LLC. on November 23, 2010. Classification: Voluntary Action Indicated (VAI).

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Record Summary

FDA Inspection 703101 for Unither Manufacturing LLC. on November 23, 2010. Classification: Voluntary Action Indicated (VAI).

Violation Codes

21 CFR 211.67(b)

21 CFR 211.68(b)

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Record Information

Company

Unither Manufacturing LLC.

Inspection Date

November 23, 2010

Product Type

Drugs

Office

Center for Drug Evaluation and Research

ID: 6cdeebcd-4f8b-481e-b044-89cc1cd32d56

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