FDA Documents of Nomax Inc
Nomax Inc is an organization that has been audited by the FDA 14 times between 2002 and 2024 across all 1 sites.
Documents
FDA 483 Nomax, Saint Louis | December 2022
Available Now - $199
Issued on: Dec 2, 2022
Human Drugs Form 483
FDA 483 Nomax Inc, Saint Louis | 2018
Out-of-stock
Issued on: Feb 1, 2018
Medical Devices & Rad Health Form 483
FDA 483 Nomax Inc, Saint Louis | 2016
Out-of-stock
Issued on: Oct 27, 2016
Human Drug Form 483
FDA 483 Nomax Inc, Saint Louis | 2012
Out-of-stock
Issued on: Jan 31, 2012
Human Drug Form 483
FDA 483 Nomax Inc, Saint Louis | 2011
Out-of-stock
Issued on: Mar 25, 2011
Human Drug Form 483
FDA 483 Nomax Inc, Saint Louis | 2008
Out-of-stock
Issued on: Jun 20, 2008
Human Drug Form 483
FDA 483 Nomax Inc, Saint Louis | 2005
Out-of-stock
Issued on: Dec 21, 2005
Human Drug Form 483
FDA 483 Nomax Inc, Saint Louis | 2004
Out-of-stock
Issued on: Aug 24, 2004
Human Drug Form 483
FDA Investigators(14)
- Eric C. Nielsen, FDA Investigator
- Robert J. Ham, FDA Investigator
- Conner N. Mann, FDA Investigator
- Shanna R. Haden, FDA Investigator
- Shafiq Ahadi, FDA Investigator
- Michele Perry-Williams, FDA Investigator
- Jeffery L. Sumter, FDA Investigator
- Michele Perry Williams, FDA Investigator
- Adree N. Anderson, FDA Investigator
- Steven D. Kehoe, FDA Investigator
- Philip J. Boston, FDA Investigator
- Erika V. Butler, FDA Investigator
- William C. Corley, FDA Investigator
- James I. Giefer, FDA Investigator