# Gynex Corporation – FDA Inspection, May 27, 2016

Source: https://www.keypedia.com/records/fda_inspections/gynex-corporation/a188bf29-d209-4c68-b1ba-d4f174b39148
Source feed: FDA_Inspections

> FDA inspection 975324 of Gynex Corporation, May 27, 2016. Classification: No Action Indicated (NAI). 6 other FDA inspections on record for this company.

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## Details

- Record Type: FDA Inspection
- Inspection ID: 975324
- Company Name: Gynex Corporation
- Inspection Date: 2016-05-27
- Classification: No Action Indicated (NAI)
- Classification Code: NAI
- Project Area: Postmarket Assurance: Devices
- Product Type: Devices
- Center: Medical Devices & Rad Health
- Office Name: Center for Devices and Radiological Health
- Citation Count: 0

## Related Documents

- FDA Inspection 1114673 - 2020-01-06
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- FDA Inspection 800085 - 2012-09-21
- FDA Inspection 791097 - 2012-07-20
- [FDA Inspection 645081 - 2010-01-21](https://www.keypedia.com/records/fda_inspections/gynex-corporation/18210e64-b7e7-477d-865f-373835c77fe7)

Company: https://www.keypedia.com/companies/gynex-corporation/3320db3d-b0e6-4488-8161-0265bdcd9b4d

Office: https://www.keypedia.com/offices/center-for-devices-and-radiological-health/9d89aff6-e435-4764-87be-f58c01aca7f7