# FDA Inspection 1059083 - Etex Corporation - July 16, 2018

Source: https://www.globalkeysolutions.net/records/fda_inspections/etex-corporation/3b3f2785-9a2b-4290-94db-89183b166f44
Source feed: FDA_Inspections

> FDA Inspection 1059083 for Etex Corporation on July 16, 2018. Classification: Voluntary Action Indicated (VAI).

---

## Details

- Record Type: FDA Inspection
- Inspection ID: 1059083
- Company Name: Etex Corporation
- Inspection Date: 2018-07-16
- Classification: Voluntary Action Indicated (VAI)
- Project Area: Compliance: Devices
- Product Type: Devices
- Office Name: Center for Devices and Radiological Health

## Related Documents

- [FDA Inspection 1250621 - 2024-09-25](https://www.globalkeysolutions.net/records/fda_inspections/etex-corporation/5b01d9b5-cef5-4695-8eb5-1fa132555379)
- [FDA Inspection 1250621 - 2024-09-25](https://www.globalkeysolutions.net/records/fda_inspections/etex-corporation/ee2c8cfa-324a-4be5-a2b0-b7ef4c10e1c1)
- [FDA Inspection 1090850 - 2019-05-23](https://www.globalkeysolutions.net/records/fda_inspections/etex-corporation/51c7b4dc-71b0-4c2b-bd64-631f8da793f9)
- [FDA Inspection 1090850 - 2019-05-23](https://www.globalkeysolutions.net/records/fda_inspections/etex-corporation/165e60eb-6ecc-4cfb-b865-603d4f4639b0)
- [FDA Inspection 1059083 - 2018-07-16](https://www.globalkeysolutions.net/records/fda_inspections/etex-corporation/debb1651-2420-4347-b723-e6491fee989b)

Company: https://www.globalkeysolutions.net/companies/etex-corporation/0026be3f-54ba-49cd-8f79-b687c9d4353b

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