# FDA Inspection 1028098 - UltraViolet Devices Inc - August 16, 2017

Source: https://www.keypedia.com/records/fda_inspections/ultraviolet-devices-inc/d3c35f9f-e22a-46bf-bc97-3ccfaf61de04
Source feed: FDA_Inspections

> FDA Inspection 1028098 for UltraViolet Devices Inc on August 16, 2017. Classification: No Action Indicated (NAI).

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## Details

- Record Type: FDA Inspection
- Inspection ID: 1028098
- Company Name: UltraViolet Devices Inc
- Inspection Date: 2017-08-16
- Classification: No Action Indicated (NAI)
- Project Area: Compliance: Devices
- Product Type: Devices
- Office Name: Center for Devices and Radiological Health

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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