# Virtex – FDA Inspection, Sep 21, 2017

Source: https://www.keypedia.com/records/fda_inspections/virtex/ca2a8961-471a-44da-bc79-d0a621bf2df7
Source feed: FDA_Inspections

> FDA inspection 1025962 of Virtex, September 21, 2017. Classification: Voluntary Action Indicated (VAI). 2 citations under 21 CFR parts 803 and 820. Form 483 issued. 2 other FDA inspections on record for this company.

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## Details

- Record Type: FDA Inspection
- Inspection ID: 1025962
- Company Name: Virtex
- Inspection Date: 2017-09-21
- 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: 2

## Related Documents

- FDA Inspection 1214397 - 2023-08-02
- [FDA Inspection 823538 - 2013-03-26](https://www.keypedia.com/records/fda_inspections/virtex/edfa3fd4-dfde-4375-a318-ead8b3342836)

## Related Officers

- [Issuing Officer](https://www.keypedia.com/people/iris-c-macinnes/5e8d7fef-18d5-453d-82b2-19e8e2897d26)
- [Issuing Officer](https://www.keypedia.com/people/jeremy-l-stukes/03812740-3c4d-4b11-9da3-44b7a03d72b1)

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