FDA Documents of Medion Diagnostics AG
Medion Diagnostics AG is an organization that has been audited by the FDA 10 times between 2000 and 2013 across all 1 sites.
Documents
FDA 483 Medion Diagnostics AG, Dudingen | 2013
Out-of-stock
Issued on: Mar 7, 2013
Biologic Form 483
FDA 483 Medion Diagnostics AG, Dudingen | 2011
Out-of-stock
Issued on: Aug 11, 2011
Medical Devices & Rad Health Form 483
FDA 483 Medion Diagnostics AG, Dudingen | 2011
Out-of-stock
Issued on: Mar 31, 2011
Biologic Form 483
FDA 483 Medion Diagnostics AG, Dudingen | 2009
Out-of-stock
Issued on: May 5, 2009
Biologic Form 483
FDA 483 Medion Diagnostics AG, Dudingen | 2007
Out-of-stock
Issued on: Mar 1, 2007
Biologic Form 483
FDA 483 Medion Diagnostics AG, Dudingen | 2007
Out-of-stock
Issued on: Feb 8, 2007
Medical Devices & Rad Health Form 483
FDA 483 Medion Diagnostics AG, Dudingen | 2004
Out-of-stock
Issued on: Nov 12, 2004
Biologic Form 483
FDA 483 Medion Diagnostics AG, Dudingen | 2004
Out-of-stock
Issued on: Apr 30, 2004
Medical Devices & Rad Health Form 483
FDA 483 Medion Diagnostics AG, Dudingen | 2002
Out-of-stock
Issued on: Aug 14, 2002
Biologic Form 483
FDA 483 Medion Diagnostics AG, Dudingen | 2000
Out-of-stock
Issued on: May 18, 2000
Biologic Form 483
FDA Investigators(9)
- Cynthia Jim, FDA Investigator
- Frank J. Marciniak, FDA Investigator
- Prabhu P. Raju, FDA Investigator
- Rose M. Ashley, FDA Investigator
- Katherine E. Jacobitz, FDA Investigator
- Omotunde O. Osunsanmi, FDA Investigator
- Steven E. Kane, FDA Investigator
- Julie D. Bringger, FDA Investigator
- Eliezer Ramos, FDA Investigator