FDA Inspection 1090360 - Unither Manufacturing LLC. - May 22, 2019

FDA Inspection 1090360 for Unither Manufacturing LLC. on May 22, 2019. Classification: Voluntary Action Indicated (VAI).

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Record Summary

FDA Inspection 1090360 for Unither Manufacturing LLC. on May 22, 2019. Classification: Voluntary Action Indicated (VAI).

Violation Codes

21 CFR 211.188(b)(2)

21 CFR 211.192

21 CFR 211.67(a)

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Record Information

Company

Unither Manufacturing LLC.

Inspection Date

May 22, 2019

Product Type

Drugs

Office

Center for Drug Evaluation and Research

ID: c62309ca-e92a-4db1-a6a5-3eff745566c1

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