# FDA Inspection 819226 - Etex Corporation - February 15, 2013

Source: https://www.globalkeysolutions.net/records/fda_inspections/etex-corporation/a2312080-55d4-4417-9e22-0f1012707475
Source feed: FDA_Inspections

> FDA Inspection 819226 for Etex Corporation on February 15, 2013. Classification: Voluntary Action Indicated (VAI).

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## Details

- Record Type: FDA Inspection
- Inspection ID: 819226
- Company Name: Etex Corporation
- Inspection Date: 2013-02-15
- 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/etex-corporation/0026be3f-54ba-49cd-8f79-b687c9d4353b

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