# FDA Inspection 680526 - Etex Corporation - September 29, 2010

Source: https://www.keypedia.com/records/fda_inspections/etex-corporation/f4c57819-0306-4ea7-af64-5c8c472f03fa
Source feed: FDA_Inspections

> FDA inspection 680526 of Etex Corporation, September 29, 2010. Classification: Voluntary Action Indicated (VAI). 1 citation under 21 CFR part 820. 5 other FDA inspections on record for this company.

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## Details

- Record Type: FDA Inspection
- Inspection ID: 680526
- Company Name: Etex Corporation
- Inspection Date: 2010-09-29
- Classification: Voluntary Action Indicated (VAI)
- Classification Code: VAI
- Project Area: Compliance: Devices
- Product Type: Devices
- Center: Medical Devices & Rad Health
- Office Name: Center for Devices and Radiological Health
- Citation Count: 1

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

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