# Virtex – FDA Inspection, Apr 19, 2024

Source: https://www.keypedia.com/records/fda_inspections/virtex/705f70ed-b80a-468e-9d8d-86cadd791783
Source feed: FDA_Inspections

> FDA inspection 1236405 of Virtex, April 19, 2024. Classification: Voluntary Action Indicated (VAI). 1 citation under 21 CFR part 820. 1 other FDA inspection on record for this company.

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## Details

- Record Type: FDA Inspection
- Inspection ID: 1236405
- Company Name: Virtex
- Inspection Date: 2024-04-19
- 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

## Related Documents

- FDA Inspection 1102921 - 2019-09-12

## Related Officers

- [Issuing Officer](https://www.keypedia.com/people/albert-l-nguyen/496338d0-71c4-43da-92f0-09515559d9fc)
- [Investigator](https://www.keypedia.com/people/brian-r-hendricks/c2759597-935c-4b48-8fc8-2d1443098cc1)

Company: https://www.keypedia.com/companies/virtex/6467c19e-8ab1-4038-a523-b5ba040310e6

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