# FDA Inspection 1275904 - MediView XR Minnesota Office - July 10, 2025

Source: https://www.keypedia.com/records/fda_inspections/mediview-xr-minnesota-office/0a4f3ea4-e061-4c8b-afca-1a59af833426
Source feed: FDA_Inspections

> FDA Inspection 1275904 for MediView XR Minnesota Office on July 10, 2025. Classification: No Action Indicated (NAI).

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## Details

- Record Type: FDA Inspection
- Inspection ID: 1275904
- Company Name: MediView XR Minnesota Office
- Inspection Date: 2025-07-10
- Classification: No Action Indicated (NAI)
- Project Area: Compliance: Devices
- Product Type: Devices
- Office Name: Center for Devices and Radiological Health

## Related Documents

- [FDA Inspection 1275904 - 2025-07-10](https://www.keypedia.com/records/fda_inspections/mediview-xr-minnesota-office/023518fc-9510-4829-bec1-be0a699cb2e3)
- [FDA Inspection 1275904 - 2025-07-10](https://www.keypedia.com/records/fda_inspections/mediview-xr-minnesota-office/a9cb5200-cc62-4b7b-ad9f-b8684bf86558)

Company: https://www.keypedia.com/companies/mediview-xr-minnesota-office/36fe48ad-3e4d-4cbc-b4ed-3777d85f7e73

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