FDA Inspection 896590 - FibroGen Incorporated - September 19, 2014

FDA Inspection 896590 for FibroGen Incorporated on September 19, 2014. Classification: Voluntary Action Indicated (VAI).

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Record Summary

FDA Inspection 896590 for FibroGen Incorporated on September 19, 2014. Classification: Voluntary Action Indicated (VAI).

Violation Codes

21 CFR 312.50

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Record Information

Company

FibroGen Incorporated

Inspection Date

September 19, 2014

Product Type

Drugs

Office

Center for Drug Evaluation and Research

ID: e7ff8b58-1cc9-4350-b6a9-12702e3dd5a5

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