FDA Inspection 952968 - Sanofi-Aventis Deutschland GmbH - December 10, 2015

FDA Inspection 952968 for Sanofi-Aventis Deutschland GmbH on December 10, 2015. Classification: No Action Indicated (NAI).

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Record Summary

FDA Inspection 952968 for Sanofi-Aventis Deutschland GmbH on December 10, 2015. Classification: No Action Indicated (NAI).

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Record Information

Company

Sanofi-Aventis Deutschland GmbH

Inspection Date

December 10, 2015

Product Type

Devices

Office

Center for Devices and Radiological Health

ID: f95612b4-5fa3-4205-a61d-3fc16648e19c

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