FDA Inspection 1275904 — MediView XR Minnesota Office
The FDA completed an inspection of MediView XR Minnesota Office on July 10, 2025 in Roseville, MN. 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
- July 10, 2025
- Fiscal Year
- 2025
- Product Type
- Devices
- Project Area
- Postmarket Assurance: Devices
- Location
- Roseville, MN (United States)