# FDA Inspection 800085 - Gynex Corporation - September 21, 2012

Source: https://www.globalkeysolutions.net/records/fda_inspections/gynex-corporation/fe90ccad-a7fd-47a2-b5c0-4c088d755c06/
Source feed: FDA_Inspections

> FDA Inspection 800085 for Gynex Corporation on September 21, 2012. Classification: No Action Indicated (NAI).

---

## Details

- Record Type: FDA Inspection
- Inspection ID: 800085
- Company Name: Gynex Corporation
- Inspection Date: 2012-09-21
- Classification: No Action Indicated (NAI)
- Project Area: Compliance: Devices
- Product Type: Devices
- Office Name: Center for Devices and Radiological Health

## Related Documents

- [FDA Inspection 1114673 - 2020-01-06](https://www.globalkeysolutions.net/api/records/fda_inspections/gynex-corporation/12296a52-e5af-4b04-964c-dcc1d82ae3e3/)
- [FDA Inspection 1114673 - 2020-01-06](https://www.globalkeysolutions.net/api/records/fda_inspections/gynex-corporation/eb7b1b53-6387-4585-865f-87329d37c128/)
- [FDA Inspection 975324 - 2016-05-27](https://www.globalkeysolutions.net/api/records/fda_inspections/gynex-corporation/323a2be2-ed3b-4148-abe3-d5ca52a18a0b/)
- [FDA Inspection 975324 - 2016-05-27](https://www.globalkeysolutions.net/api/records/fda_inspections/gynex-corporation/a188bf29-d209-4c68-b1ba-d4f174b39148/)
- [FDA Inspection 876242 - 2014-04-25](https://www.globalkeysolutions.net/api/records/fda_inspections/gynex-corporation/b6be5851-24d7-42a7-9231-93fa094bff22/)

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

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