# FDA Inspection 1267055 - Innovize Inc - March 26, 2025

Source: https://www.keypedia.com/records/fda_inspections/innovize-inc/84c8a543-da5b-4f7c-a22a-975605b7253f
Source feed: FDA_Inspections

> FDA Inspection 1267055 for Innovize Inc on March 26, 2025. Classification: No Action Indicated (NAI).

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## Details

- Record Type: FDA Inspection
- Inspection ID: 1267055
- Company Name: Innovize Inc
- Inspection Date: 2025-03-26
- Classification: No Action Indicated (NAI)
- Project Area: Postmarket Assurance: Medical Devices
- Product Type: Medical Devices & Rad Health
- Office Name: Minneapolis District Office

## Related Documents

- [FDA Inspection 1267055 - 2025-03-26](https://www.keypedia.com/records/fda_inspections/innovize-inc/ff425221-ed44-4ec5-bb6c-4ca2dce3ba92)
- [FDA Inspection 1267055 - 2025-03-26](https://www.keypedia.com/records/fda_inspections/innovize-inc/3868b7e7-2967-4e2d-b070-44bdcb36d6c1)
- [FDA Inspection 1267055 - 2025-03-26](https://www.keypedia.com/records/fda_inspections/innovize-inc/1c96579c-e882-4f54-938f-081d8cc6a3a0)
- [FDA Inspection 958727 - 2016-01-21](https://www.keypedia.com/records/fda_inspections/innovize-inc/7a41b8f0-dcb0-4b16-abc9-a0d67e9a616c)

Company: https://www.keypedia.com/companies/innovize-inc/f397ecf8-bc00-4d99-96ab-7d15bf205dd5

Office: https://www.keypedia.com/offices/minneapolis-district-office/c79fc8dc-f884-48fc-ba80-2947f662511d