# FDA Inspection 1025962 - Virtex - September 21, 2017

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

> FDA Inspection 1025962 for Virtex on September 21, 2017. Classification: Voluntary Action Indicated (VAI).

---

## Details

- Record Type: FDA Inspection
- Inspection ID: 1025962
- Company Name: Virtex
- Inspection Date: 2017-09-21
- Classification: Voluntary Action Indicated (VAI)
- Project Area: Compliance: Devices
- Product Type: Devices
- Office Name: Center for Devices and Radiological Health

## Related Documents

- [FDA Inspection 1214397 - 2023-08-02](https://www.keypedia.com/records/fda_inspections/virtex/7e87121c-4425-4480-9e25-4f9461bbda8f)
- [FDA Inspection 1214397 - 2023-08-02](https://www.keypedia.com/records/fda_inspections/virtex/5e84ee7c-c1d6-411f-9352-eb2547b642c7)
- [FDA Inspection 823538 - 2013-03-26](https://www.keypedia.com/records/fda_inspections/virtex/edfa3fd4-dfde-4375-a318-ead8b3342836)
- [FDA Inspection 823538 - 2013-03-26](https://www.keypedia.com/records/fda_inspections/virtex/e1ff9294-d76e-4ca4-85e6-c0e5033c80dd)

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