# FDA Inspection 1280195 - MediView XR Inc. - August 26, 2025

Source: https://www.keypedia.com/records/fda_inspections/mediview-xr-inc/aec40f08-7f96-46ee-83c0-baee62becfad
Source feed: FDA_Inspections

> FDA Inspection 1280195 for MediView XR Inc. on August 26, 2025. Classification: No Action Indicated (NAI).

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## Details

- Record Type: FDA Inspection
- Inspection ID: 1280195
- Company Name: MediView XR Inc.
- Inspection Date: 2025-08-26
- Classification: No Action Indicated (NAI)
- Project Area: Postmarket Assurance: Devices
- Product Type: Devices
- Office Name: Center for Devices and Radiological Health

## Related Documents

- [FDA Inspection 1280195 - 2025-08-26](https://www.keypedia.com/records/fda_inspections/mediview-xr-inc/e2302ce7-0b38-4330-9f00-b45cc603cdc9)
- [FDA Inspection 1280195 - 2025-08-26](https://www.keypedia.com/records/fda_inspections/mediview-xr-inc/8195c39d-45eb-402a-ad0b-3011878a287e)

Company: https://www.keypedia.com/companies/mediview-xr-inc/1b893ca9-fbc1-4dd1-b5bc-0dee2d902f3b

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