FDA Documents of Sanofi-Aventis Deutschland GmbH

Sanofi-Aventis Deutschland GmbH is an organization that has been audited by the FDA 20 times between 2002 and 2022 across all 7 sites.

Documents

FDA 483 Sanofi-Aventis Deutschland GmbH, Frankfurt Am Main | 2019

Out-of-stock
Issued on: May 14, 2019
Human Drug Form 483

FDA 483 Sanofi-Aventis Deutschland GmbH, Frankfurt am Main | 2017

Out-of-stock
Issued on: Mar 3, 2017
Human Drug Form 483

FDA 483 Sanofi-Aventis Deutschland GmbH, Frankfurt am Main | 2015

Out-of-stock
Issued on: Jun 26, 2015
Human Drug Form 483

FDA 483 Sanofi-Aventis Deutschland GmbH, Frankfurt am Main | 2013

Out-of-stock
Issued on: Jul 2, 2013
Medical Devices & Rad Health Form 483

FDA 483 Sanofi-Aventis Deutschland GmbH, Frankfurt am Main | 2013

Out-of-stock
Issued on: Jul 2, 2013
Medical Devices & Rad Health Form 483

FDA 483 Sanofi-Aventis Deutschland GmbH, Frankfurt am Main | 2011

Out-of-stock
Issued on: Jul 14, 2011
Human Drug Form 483

FDA 483 Sanofi-Aventis Deutschland GmbH, Frankfurt am Main | 2010

Out-of-stock
Issued on: Sep 16, 2010
Human Drug Form 483

FDA 483 Sanofi-Aventis Deutschland GmbH, Frankfurt am Main | 2008

Out-of-stock
Issued on: Oct 31, 2008
Human Drug Form 483

FDA 483 Sanofi-Aventis Deutschland GmbH, Frankfurt am Main | 2005

Out-of-stock
Issued on: Nov 4, 2005
Human Drug Form 483

FDA 483 Sanofi-Aventis Deutschland GmbH, Frankfurt am Main | 2005

Out-of-stock
Issued on: Jun 27, 2005
Human Drug Form 483

FDA 483 Sanofi-Aventis Deutschland GmbH, Frankfurt am Main | 2003

Out-of-stock
Issued on: Sep 22, 2003
Human Drug Form 483