FDA Inspection 859523 - Sanofi-Aventis Deutschland GmbH - December 05, 2013

FDA Inspection 859523 for Sanofi-Aventis Deutschland GmbH on December 05, 2013. Classification: No Action Indicated (NAI).

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Record Summary

FDA Inspection 859523 for Sanofi-Aventis Deutschland GmbH on December 05, 2013. Classification: No Action Indicated (NAI).

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Record Information

Company

Sanofi-Aventis Deutschland GmbH

Inspection Date

December 5, 2013

Product Type

Drugs

Office

Center for Drug Evaluation and Research

ID: fbf8c89d-da33-4f7d-befb-9dc5e07d556d

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