# FDA Inspection 1284836 - RadiusXR, Inc. - September 10, 2025

Source: https://www.keypedia.com/records/fda_inspections/radiusxr-inc/9d4ca44f-3633-422d-a4c0-8f0cb7bf3ee1
Source feed: FDA_Inspections

> FDA Inspection 1284836 for RadiusXR, Inc. on September 10, 2025. Classification: No Action Indicated (NAI).

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## Details

- Record Type: FDA Inspection
- Inspection ID: 1284836
- Company Name: RadiusXR, Inc.
- Inspection Date: 2025-09-10
- Classification: No Action Indicated (NAI)
- Project Area: Compliance: Devices
- Product Type: Devices
- Office Name: Center for Devices and Radiological Health

## Related Documents

- [FDA Inspection 1284836 - 2025-09-10](https://www.keypedia.com/records/fda_inspections/radiusxr-inc/b2ec06fe-26bd-45c2-81eb-a405bef3e97e)
- [FDA Inspection 1284836 - 2025-09-10](https://www.keypedia.com/records/fda_inspections/radiusxr-inc/f353002f-c71d-4990-9909-1035d1f8cf33)

Company: https://www.keypedia.com/companies/radiusxr-inc/e5331fe7-2033-41c7-b411-e7215aebc918

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