FDA Documents of Gynex Corporation
Gynex Corporation is an organization that has been audited by the FDA 9 times between 2006 and 2020 across all 2 sites.
Documents
FDA 483 Gynex, Redmond | April 2014
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Issued on: Apr 25, 2014
Medical Devices & Rad Health Form 483
FDA 483 Gynex Corporation, Redmond | 2020
Out-of-stock
Issued on: Jan 6, 2020
Medical Devices & Rad Health Form 483
FDA 483 Gynex Corporation, Redmond | 2016
Out-of-stock
Issued on: May 27, 2016
Medical Devices & Rad Health Form 483
FDA 483 Gynex Corporation, Redmond | 2012
Out-of-stock
Issued on: Jul 20, 2012
Medical Devices & Rad Health Form 483
FDA 483 Gynex Corporation, Redmond | 2010
Out-of-stock
Issued on: Jan 21, 2010
Human Drug Form 483
FDA 483 Gynex Corporation, Redmond | 2009
Out-of-stock
Issued on: Mar 10, 2009
Human Drug Form 483
FDA 483 Gynex Corporation, Redmond | 2008
Out-of-stock
Issued on: May 23, 2008
Medical Devices & Rad Health Form 483
FDA Investigators(11)
- James A. Lane, FDA Investigator
- Paul M. Kawamoto, FDA Investigator
- Kun C. Liu, FDA Investigator
- Stephen R. Souza, FDA Investigator
- Sharon I. Gundersen, FDA Investigator
- Heika R. Tait, FDA Investigator
- Maria P. Kelly-Doggett, FDA Investigator
- S. L. Brown, FDA Investigator
- Brown, S. L, FDA Investigator
- Catherine J. Laufmann, FDA Investigator
- Lori J. Silverstein, FDA Investigator