FDA Inspection 1284836 — RadiusXR, Inc.

RadiusXR, Inc. — FEI 3014397047

The FDA completed an inspection of RadiusXR, Inc. on September 10, 2025 in Pleasanton, CA. The inspection was classified NAI (No Action Indicated — no objectionable conditions were found). Product area: Devices.

Inspection Details

Classification
No Action Indicated (NAI) (NAI)
End Date
September 10, 2025
Fiscal Year
2025
Product Type
Devices
Project Area
Compliance: Devices
Location
Pleasanton, CA (United States)