FDA Documents of Greiner Bio-One North America, Inc.
Greiner Bio-One North America, Inc. is an organization that has been audited by the FDA 9 times between 2003 and 2023 across all 1 sites.
Documents
FDA 483 Greiner Bio-One North America, Monroe | October 2021
Available Now - $199
Issued on: Oct 29, 2021
Medical Devices & Rad Health Form 483
FDA 483 Greiner Bio-One North America, Monroe | Dec 2019
Available Now - $199
Issued on: Dec 13, 2019
Medical Devices & Rad Health Form 483
FDA EIR Greiner Bio-One North America, Monroe | Dec 2019
Available Now - $995
Issued on: Dec 13, 2019
Medical Devices & Rad Health Form 483
FDA 483 Greiner Bio-One North America, Inc., Monroe | 2017
Out-of-stock
Issued on: Aug 17, 2017
Medical Devices & Rad Health Form 483
FDA 483 Greiner Bio-One North America, Inc., Monroe | 2013
Out-of-stock
Issued on: Jul 24, 2013
Medical Devices & Rad Health Form 483
FDA 483 Greiner Bio-One North America, Inc., Monroe | 2006
Out-of-stock
Issued on: Aug 9, 2006
Medical Devices & Rad Health Form 483
FDA 483 Greiner Bio-One North America, Inc., Monroe | 2003
Out-of-stock
Issued on: Nov 20, 2003
Medical Devices & Rad Health Form 483
FDA Investigators(13)
- Christopher B. May, FDA Investigator
- Inga M. Warr, FDA Investigator
- Melanie W. Pishnery, FDA Investigator
- Edward E. Lockwood, FDA Investigator
- David E. Lowe, FDA Investigator
- Matthew A. Humbard, FDA Investigator
- Gamal A. Norton, FDA Investigator
- Claudette D. Brooks, FDA Investigator
- Ernest H. Blackwood, FDA Investigator
- Trang N. Cox, FDA Investigator
- Ibad U. Khan, FDA Investigator
- Sarah M. Forney, FDA Investigator
- George T. Allen, FDA Investigator