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

Source: https://www.globalkeysolutions.net/records/fda_inspections/sanofi-aventis-deutschland-gmbh/f95612b4-5fa3-4205-a61d-3fc16648e19c/
Source feed: FDA_Inspections

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

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## Details

- Record Type: FDA Inspection
- Inspection ID: 952968
- Company Name: Sanofi-Aventis Deutschland GmbH
- Inspection Date: 2015-12-10
- Classification: No Action Indicated (NAI)
- Project Area: Compliance: Devices
- Product Type: Devices
- Office Name: Center for Devices and Radiological Health

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Company: https://www.globalkeysolutions.net/companies/sanofi-aventis-deutschland-gmbh/07c96432-bb43-45e5-a80d-e4bca284dbab

Office: https://www.globalkeysolutions.net/offices/center-for-devices-and-radiological-health/9d89aff6-e435-4764-87be-f58c01aca7f7