# Sanofi-Aventis Deutschland GmbH - Inspection Records

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

> Inspection records and compliance data for Sanofi-Aventis Deutschland GmbH in Frankfurt Am Main, None. Access full analysis and detailed observations.

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## Details

- Name: Sanofi-Aventis Deutschland GmbH
- FEI Number: 3003195501
- City: Frankfurt Am Main
- State: None
- Country Name: Germany
- Address Line 1: Industriepark Hochst, Bruningstr. 50
- Zip Code: None
- Business Operations: API MANUFACTURE, API/FDF ANALYTICAL TESTING, FDF MANUFACTURE, PACK

## Related Documents

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- [FDA Inspection 1215824 - Sanofi-Aventis Deutschland GmbH - 2022-03-25](https://www.keypedia.com/records/fda_inspections/sanofi-aventis-deutschland-gmbh/0f7ed7fe-fb9c-46e0-bb70-178a3f78e97a) — classification: Voluntary Action Indicated (VAI), source: FDA, date: March 25, 2022
- [FDA Inspection 1094836 - Sanofi-Aventis Deutschland GmbH - 2019-05-14](https://www.keypedia.com/records/fda_inspections/sanofi-aventis-deutschland-gmbh/8ee42dad-b559-446f-9c69-d3ad6a8d8521) — classification: Voluntary Action Indicated (VAI), source: FDA, date: May 14, 2019
- [FDA Inspection 1006001 - Sanofi-Aventis Deutschland GmbH - 2017-03-03](https://www.keypedia.com/records/fda_inspections/sanofi-aventis-deutschland-gmbh/c34bec9c-4453-44d0-bcba-d9df811b7c10) — classification: Voluntary Action Indicated (VAI), source: FDA, date: March 3, 2017
- [FDA Inspection 952968 - Sanofi-Aventis Deutschland GmbH - 2015-12-10](https://www.keypedia.com/records/fda_inspections/sanofi-aventis-deutschland-gmbh/f95612b4-5fa3-4205-a61d-3fc16648e19c) — classification: No Action Indicated (NAI), source: FDA, date: December 10, 2015
- [FDA Inspection 933399 - Sanofi-Aventis Deutschland GmbH - 2015-06-26](https://www.keypedia.com/records/fda_inspections/sanofi-aventis-deutschland-gmbh/30e13d35-ce61-4715-bf92-a25d0baac382) — classification: Voluntary Action Indicated (VAI), source: FDA, date: June 26, 2015
- [FDA Inspection 859523 - Sanofi-Aventis Deutschland GmbH - 2013-12-05](https://www.keypedia.com/records/fda_inspections/sanofi-aventis-deutschland-gmbh/fbf8c89d-da33-4f7d-befb-9dc5e07d556d) — classification: No Action Indicated (NAI), source: FDA, date: December 5, 2013
- [FDA Inspection 841970 - Sanofi-Aventis Deutschland GmbH - 2013-07-02](https://www.keypedia.com/records/fda_inspections/sanofi-aventis-deutschland-gmbh/706cca2f-8081-432e-863e-520ce7639bdd) — classification: Voluntary Action Indicated (VAI), source: FDA, date: July 2, 2013
- [FDA Inspection 841970 - Sanofi-Aventis Deutschland GmbH - 2013-07-02](https://www.keypedia.com/records/fda_inspections/sanofi-aventis-deutschland-gmbh/1c2c86b4-8ab1-4cba-b81a-cff930ec85c2) — classification: Voluntary Action Indicated (VAI), source: FDA, date: July 2, 2013
- [FDA Inspection 841970 - Sanofi-Aventis Deutschland GmbH - 2013-07-02](https://www.keypedia.com/records/fda_inspections/sanofi-aventis-deutschland-gmbh/465232d2-bbb5-42f1-a417-4741d0577b29) — classification: Voluntary Action Indicated (VAI), source: FDA, date: July 2, 2013

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