FDA Documents of Kerr/Pentron, DBA Kerr Corporation and Pentron Clinical
Kerr/Pentron, DBA Kerr Corporation and Pentron Clinical is an organization that has been audited by the FDA 7 times between 2001 and 2020 across all 1 sites.
Documents
FDA 483 Kerr/Pentron, DBA Kerr Corporation and Pentron Clinical, Orange | 2020
Out-of-stock
Issued on: Jun 16, 2020
Medical Devices & Rad Health Form 483
FDA 483 Kerr/Pentron, DBA Kerr Corporation and Pentron Clinical, Orange | 2017
Out-of-stock
Issued on: Jul 12, 2017
Medical Devices & Rad Health Form 483
FDA 483 Kerr/Pentron, DBA Kerr Corporation and Pentron Clinical, Orange | 2015
Out-of-stock
Issued on: Oct 21, 2015
Medical Devices & Rad Health Form 483
FDA 483 Kerr/Pentron, DBA Kerr Corporation and Pentron Clinical, Orange | 2011
Out-of-stock
Issued on: Nov 8, 2011
Medical Devices & Rad Health Form 483
FDA 483 Kerr/Pentron, DBA Kerr Corporation and Pentron Clinical, Orange | 2004
Out-of-stock
Issued on: Feb 23, 2004
Medical Devices & Rad Health Form 483
FDA Investigators (10)
- MDSAP harperd, FDA Investigator
- MDSAP WilliamsA, FDA Investigator
- MSDAP GonzlezK, FDA Investigator
- MDSAP GonzlezK, FDA Investigator
- Kimberly M. Lichter, FDA Investigator
- Trudy R. Papson, FDA Investigator
- Herminio C. Francisco, FDA Investigator
- Selene T. Torres, FDA Investigator
- Jocelyn E. Massey, FDA Investigator
- Lanita F. Kelley, FDA Investigator