# FDA Inspection 1102921 - Virtex - September 12, 2019

Source: https://www.keypedia.com/records/fda_inspections/virtex/39210910-a202-43f1-876d-ee14e8303d8e
Source feed: FDA_Inspections

> FDA Inspection 1102921 for Virtex on September 12, 2019. Classification: No Action Indicated (NAI).

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## Details

- Record Type: FDA Inspection
- Inspection ID: 1102921
- Company Name: Virtex
- Inspection Date: 2019-09-12
- Classification: No Action Indicated (NAI)
- Project Area: Compliance: Devices
- Product Type: Devices
- Office Name: Center for Devices and Radiological Health

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- [FDA Inspection 1236405 - 2024-04-19](https://www.keypedia.com/records/fda_inspections/virtex/705f70ed-b80a-468e-9d8d-86cadd791783)

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