FDA Documents of Remel, Inc
Remel, Inc is an organization that has been audited by the FDA 14 times between 2001 and 2023 across all 2 sites.
Documents
FDA 483 Remel, Oakwood Village | April 2017
Available Now - $199
Issued on: Apr 12, 2017
Medical Devices & Rad Health Form 483
FDA 483 Remel, Inc, Oakwood Village | 2019
Out-of-stock
Issued on: Nov 20, 2019
Medical Devices & Rad Health Form 483
FDA 483 Remel, Inc, Lenexa | 2015
Out-of-stock
Issued on: Oct 23, 2015
Medical Devices & Rad Health Form 483
FDA 483 Remel, Inc, Lenexa | 2014
Out-of-stock
Issued on: Jul 3, 2014
Medical Devices & Rad Health Form 483
FDA 483 Remel, Inc, Lenexa | 2013
Out-of-stock
Issued on: Jun 25, 2013
Medical Devices & Rad Health Form 483
FDA 483 Remel, Inc, Lenexa | 2010
Out-of-stock
Issued on: Mar 18, 2010
Medical Devices & Rad Health Form 483
FDA 483 Remel, Inc, Lenexa | 2007
Out-of-stock
Issued on: Nov 30, 2007
Medical Devices & Rad Health Form 483
FDA 483 Remel, Inc, Lenexa | 2005
Out-of-stock
Issued on: Dec 2, 2005
Medical Devices & Rad Health Form 483
FDA 483 Remel, Inc, Lenexa | 2001
Out-of-stock
Issued on: May 30, 2001
Medical Devices & Rad Health Form 483
FDA Investigators(15)
- Eric C. Fox, FDA Investigator
- Rosanna M. Goodrich, FDA Investigator
- Laureen M. Geniusz, FDA Investigator
- Jonathan R. Campos, FDA Investigator
- Matthew J. Morrison, FDA Investigator
- Lori Gioia, FDA Investigator
- James D. Planchon, FDA Investigator
- Bonnie E. Pierson, FDA Investigator
- Kelly D. Sheppard, FDA Investigator
- Matthew P. Barnard, FDA Investigator
- Lisa L. Gilliam, FDA Investigator
- Kara L. Roden, FDA Investigator
- Matthew A. Walburger, FDA Investigator
- Minerva Rogers, FDA Investigator
- Nadine J. Nanko, FDA Investigator