# FDA Inspection 1214397 - Virtex - August 02, 2023

Source: https://www.keypedia.com/records/fda_inspections/virtex/7e87121c-4425-4480-9e25-4f9461bbda8f
Source feed: FDA_Inspections

> FDA Inspection 1214397 for Virtex on August 02, 2023. Classification: No Action Indicated (NAI).

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## Details

- Record Type: FDA Inspection
- Inspection ID: 1214397
- Company Name: Virtex
- Inspection Date: 2023-08-02
- Classification: No Action Indicated (NAI)
- Project Area: Compliance: Devices
- Product Type: Devices
- Office Name: Center for Devices and Radiological Health

## Related Documents

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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