FDA Documents of Pierre Fabre Medicament Production

Pierre Fabre Medicament Production is an organization that has been audited by the FDA 14 times between 2001 and 2019 across all 2 sites.

Documents

FDA 483 Pierre Fabre Medicament Production, Idron | 2015

Out-of-stock
Issued on: Jun 10, 2015
Human Drug Form 483

FDA 483 Pierre Fabre Medicament Production, Idron | 2013

Out-of-stock
Issued on: Feb 26, 2013
Human Drug Form 483

FDA 483 Pierre Fabre Medicament Production, Idron | 2013

Out-of-stock
Issued on: Feb 26, 2013
Human Drug Form 483

FDA 483 Pierre Fabre Medicament Production, Idron | 2011

Out-of-stock
Issued on: May 12, 2011
Human Drug Form 483

FDA 483 Pierre Fabre Medicament Production, Idron | 2009

Out-of-stock
Issued on: Sep 8, 2009
Human Drug Form 483

FDA 483 Pierre Fabre Medicament Production, Idron | 2006

Out-of-stock
Issued on: Apr 6, 2006
Human Drug Form 483

FDA 483 Pierre Fabre Medicament Production, Idron | 2004

Out-of-stock
Issued on: Mar 9, 2004
Human Drug Form 483

FDA 483 Pierre Fabre Medicament Production, Idron | 2003

Out-of-stock
Issued on: Jul 1, 2003
Biologic Form 483

FDA 483 Pierre Fabre Medicament Production, Idron | 2002

Out-of-stock
Issued on: Mar 15, 2002
Biologic Form 483

FDA 483 Pierre Fabre Medicament Production, Idron | 2001

Out-of-stock
Issued on: Nov 30, 2001
Human Drug Form 483

FDA 483 Pierre Fabre Medicament Production, Idron | 2001

Out-of-stock
Issued on: May 11, 2001
Biologic Form 483