FDA Inspection
Gynex CorporationGynex Corporation – FDA Inspection, May 27, 2016
Record Details
This FDA Inspection record concerns Gynex Corporation, with an inspection on May 27, 2016, issued by the Center for Devices and Radiological Health, covering devices.
- Company
- Gynex Corporation
- Inspection Date
- May 27, 2016
- Product Type
- Devices
View Company Profile
ID · a188bf29-d209-4c68-b1ba-d4f174b39148
Inspection Facts
No Action Indicated (NAI)
No objectionable conditions or practices were found during the inspection.
- Inspection number
- 975324
- FDA center
- Medical Devices & Rad Health
- Project area
- Postmarket Assurance: Devices
Other FDA inspections of Gynex Corporation
6| Date | Classification | Office | Project area |
|---|---|---|---|
| January 6, 2020 | VAI | Center for Devices and Radiological Health | Compliance: Devices |
| April 25, 2014 | NAI | Center for Devices and Radiological Health | Postmarket Assurance: Devices |
| September 21, 2012 | NAI | Center for Devices and Radiological Health | Compliance: Devices |
| July 20, 2012 | VAI | Center for Devices and Radiological Health | Compliance: Devices |
| January 21, 2010 | VAI | Center for Drug Evaluation and Research | Drug Quality Assurance |
Other documents for Gynex Corporation
- FDA Inspection 1114673 - 2020-01-06
- FDA Inspection 876242 - 2014-04-25
- FDA Inspection 800085 - 2012-09-21
- FDA Inspection 791097 - 2012-07-20
- FDA Inspection 645081 - 2010-01-21
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