# FDA Inspection 1180555 - UltraViolet Devices Inc - September 08, 2022

Source: https://www.keypedia.com/records/fda_inspections/ultraviolet-devices-inc/d7e9ff79-40cd-4f3f-b678-b8544890be4c
Source feed: FDA_Inspections

> FDA Inspection 1180555 for UltraViolet Devices Inc on September 08, 2022. Classification: Voluntary Action Indicated (VAI).

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## Details

- Record Type: FDA Inspection
- Inspection ID: 1180555
- Company Name: UltraViolet Devices Inc
- Inspection Date: 2022-09-08
- Classification: Voluntary Action Indicated (VAI)
- Project Area: Compliance: Devices
- Product Type: Devices
- Office Name: Center for Devices and Radiological Health

## Related Documents

- [FDA Inspection 1180555 - 2022-09-08](https://www.keypedia.com/records/fda_inspections/ultraviolet-devices-inc/1dbfc9e4-76c9-418a-b8e0-07afe6afa7b6)
- [FDA Inspection 1028098 - 2017-08-16](https://www.keypedia.com/records/fda_inspections/ultraviolet-devices-inc/d3c35f9f-e22a-46bf-bc97-3ccfaf61de04)

Company: https://www.keypedia.com/companies/ultraviolet-devices-inc/8b798690-93ee-4b8e-b967-2d69f6e18176

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