FDA Inspection 940802 - The Ritedose Corporation - July 31, 2015

FDA Inspection 940802 for The Ritedose Corporation on July 31, 2015. Classification: Voluntary Action Indicated (VAI).

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Record Summary

FDA Inspection 940802 for The Ritedose Corporation on July 31, 2015. Classification: Voluntary Action Indicated (VAI).

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Record Information

Company

The Ritedose Corporation

Inspection Date

July 31, 2015

Product Type

Drugs

Office

Center for Drug Evaluation and Research

ID: 5bb61712-818a-4700-93d5-ceebb3196e83

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