FDA Inspection 1015894 - The Ritedose Corporation - March 03, 2017

FDA Inspection 1015894 for The Ritedose Corporation on March 03, 2017. Classification: Voluntary Action Indicated (VAI).

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Record Summary

FDA Inspection 1015894 for The Ritedose Corporation on March 03, 2017. Classification: Voluntary Action Indicated (VAI).

Violation Codes

21 CFR 211.160(a)

21 CFR 820.100(b)

21 CFR 820.20(b)

21 CFR 820.20(c)

21 CFR 820.30(j)

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Record Information

Company

The Ritedose Corporation

Inspection Date

March 3, 2017

Product Type

Drugs

Office

Center for Drug Evaluation and Research

ID: a5ca351d-8c5a-491e-9500-e6796c673502

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