# Virtex – FDA Inspection, Mar 26, 2013

Source: https://www.keypedia.com/records/fda_inspections/virtex/edfa3fd4-dfde-4375-a318-ead8b3342836
Source feed: FDA_Inspections

> FDA inspection 823538 of Virtex, March 26, 2013. Classification: Voluntary Action Indicated (VAI). 4 citations under 21 CFR part 820. 2 other FDA inspections on record for this company.

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## Details

- Record Type: FDA Inspection
- Inspection ID: 823538
- Company Name: Virtex
- Inspection Date: 2013-03-26
- Classification: Voluntary Action Indicated (VAI)
- Classification Code: VAI
- Project Area: Postmarket Assurance: Devices
- Product Type: Devices
- Center: Medical Devices & Rad Health
- Office Name: Center for Devices and Radiological Health
- Citation Count: 4

## Related Documents

- FDA Inspection 1214397 - 2023-08-02
- [FDA Inspection 1025962 - 2017-09-21](https://www.keypedia.com/records/fda_inspections/virtex/ca2a8961-471a-44da-bc79-d0a621bf2df7)

Company: https://www.keypedia.com/companies/virtex/de871f9d-5f39-48af-a2f5-e1a3c461e468

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