FDA Documents of Philips Medizin Systeme Boeblingen Gmbh
Philips Medizin Systeme Boeblingen Gmbh is an organization that has been audited by the FDA 10 times between 2000 and 2024 across all 2 sites.
Documents
FDA 483 Philips Medizin Systeme Boeblingen Gmbh, Boblingen | 2017
Out-of-stock
Issued on: Nov 24, 2017
Medical Devices & Rad Health Form 483
FDA 483 Philips Medizin Systeme Boeblingen Gmbh, Boblingen | 2015
Out-of-stock
Issued on: Jan 29, 2015
Medical Devices & Rad Health Form 483
FDA 483 Philips Medizin Systeme Boeblingen Gmbh, Boblingen | 2015
Out-of-stock
Issued on: Jan 29, 2015
Medical Devices & Rad Health Form 483
FDA 483 Philips Medizin Systeme Boeblingen Gmbh, Boblingen | 2012
Out-of-stock
Issued on: Jun 14, 2012
Medical Devices & Rad Health Form 483
FDA 483 Philips Medizin Systeme Boeblingen Gmbh, Boblingen | 2010
Out-of-stock
Issued on: Sep 23, 2010
Medical Devices & Rad Health Form 483
FDA 483 Philips Medizin Systeme Boeblingen Gmbh, Boblingen | 2004
Out-of-stock
Issued on: Nov 18, 2004
Medical Devices & Rad Health Form 483
FDA 483 Philips Medizin Systeme Boeblingen Gmbh, Boblingen | 2000
Out-of-stock
Issued on: Jun 6, 2000
Medical Devices & Rad Health Form 483
FDA Investigators(9)
- Katarzyna Plona, FDA Investigator
- MDSAP WilliamsA, FDA Investigator
- Stephen C. Smith, FDA Investigator
- Catherine J. Laufmann, FDA Investigator
- Sergio Chavez, FDA Investigator
- Perry H. Gambrell, FDA Investigator
- Victor Spanioli, FDA Investigator
- David P. Vanhouten, FDA Investigator
- Mark E. Chan, FDA Investigator