# FDA Inspection 1222755 - UltraRad Corporation - August 18, 2023

Source: https://www.keypedia.com/records/fda_inspections/ultrarad-corporation/cc4327c2-4b2e-4506-8b42-8a7075e65ae6
Source feed: FDA_Inspections

> FDA Inspection 1222755 for UltraRad Corporation on August 18, 2023. Classification: No Action Indicated (NAI).

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## Details

- Record Type: FDA Inspection
- Inspection ID: 1222755
- Company Name: UltraRad Corporation
- Inspection Date: 2023-08-18
- Classification: No Action Indicated (NAI)
- Project Area: Postmarket Assurance: Devices
- Product Type: Devices
- Office Name: Center for Devices and Radiological Health

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Company: https://www.keypedia.com/companies/ultrarad-corporation/ac29a227-eea9-4dc8-8b5b-b8c1695020ba

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