FDA Documents of Nordmark Arzneimittel GMBH & Co. KG
Nordmark Arzneimittel GMBH & Co. KG is an organization that has been audited by the FDA 8 times between 2008 and 2023 across all 1 sites.
Documents
FDA 483 Nordmark Arzneimittel GMBH & Co. KG, Uetersen | 2019
Out-of-stock
Issued on: Aug 16, 2019
Human Drug Form 483
FDA 483 Nordmark Arzneimittel GMBH & Co. KG, Uetersen | 2017
Out-of-stock
Issued on: Feb 17, 2017
Human Drug Form 483
FDA 483 Nordmark Arzneimittel GMBH & Co. KG, Uetersen | 2014
Out-of-stock
Issued on: Nov 20, 2014
Human Drug Form 483
FDA 483 Nordmark Arzneimittel GMBH & Co. KG, Uetersen | 2012
Out-of-stock
Issued on: Nov 29, 2012
Human Drug Form 483
FDA 483 Nordmark Arzneimittel GMBH & Co. KG, Uetersen | 2009
Out-of-stock
Issued on: Apr 9, 2009
Human Drug Form 483
FDA 483 Nordmark Arzneimittel GMBH & Co. KG, Uetersen | 2008
Out-of-stock
Issued on: Jun 19, 2008
Human Drug Form 483
FDA Investigators(9)
- MRA MunizN, FDA Investigator
- Charles L. Zhou, FDA Investigator
- Lucila B. Nwatu, FDA Investigator
- Timothy T. Kapsala, FDA Investigator
- Michele L. Obert, FDA Investigator
- Yumi J. Hiramine, FDA Investigator
- Gwyn G. Dickinson, FDA Investigator
- Felix Maldonado, FDA Investigator
- Paraluman S. Leonin, FDA Investigator