# FDA Inspection 841970 - Sanofi-Aventis Deutschland GmbH - July 02, 2013

Source: https://www.keypedia.com/records/fda_inspections/sanofi-aventis-deutschland-gmbh/1c2c86b4-8ab1-4cba-b81a-cff930ec85c2
Source feed: FDA_Inspections

> FDA Inspection 841970 for Sanofi-Aventis Deutschland GmbH on July 02, 2013. Classification: Voluntary Action Indicated (VAI).

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## Details

- Record Type: FDA Inspection
- Inspection ID: 841970
- Company Name: Sanofi-Aventis Deutschland GmbH
- Inspection Date: 2013-07-02
- Classification: Voluntary Action Indicated (VAI)
- Project Area: Compliance: Devices
- Product Type: Devices
- Office Name: Center for Devices and Radiological Health

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

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