# FDA Inspection 975324 - Gynex Corporation - May 27, 2016

Source: https://www.globalkeysolutions.net/records/fda_inspections/gynex-corporation/323a2be2-ed3b-4148-abe3-d5ca52a18a0b
Source feed: FDA_Inspections

> FDA Inspection 975324 for Gynex Corporation on May 27, 2016. Classification: Voluntary Action Indicated (VAI).

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## Details

- Record Type: FDA Inspection
- Inspection ID: 975324
- Company Name: Gynex Corporation
- Inspection Date: 2016-05-27
- Classification: Voluntary Action Indicated (VAI)
- Project Area: Compliance: Devices
- Product Type: Devices
- Office Name: Center for Devices and Radiological Health

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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