# FDA Inspection 1236405 - Virtex - April 19, 2024

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

> FDA Inspection 1236405 for Virtex on April 19, 2024. Classification: Voluntary Action Indicated (VAI).

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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)
- Project Area: Compliance: Devices
- Product Type: Devices
- Office Name: Center for Devices and Radiological Health

## Related Documents

- [FDA Inspection 1102921 - 2019-09-12](https://www.keypedia.com/records/fda_inspections/virtex/39210910-a202-43f1-876d-ee14e8303d8e)

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