# FDA 483 - Innovize Inc - March 26, 2025

Source: https://www.keypedia.com/records/483/innovize-inc/4ed6f523-1a82-4099-84a7-e6de9c34c259

> FDA 483 for Innovize Inc on March 26, 2025. Product: device. Access full analysis and detailed observations.

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## Details

- Record Type: 483
- Company Name: Innovize Inc
- Inspection Date: 2025-03-26
- Product Type: device
- Office Name: Minneapolis District Office
- Summary: An FDA inspection of Innovize LLC, a contract manufacturer in St Paul, MN, revealed two significant observations. The firm failed to include required information, specifically dates of investigation, in complaint records and its procedures did not mandate this documentation. Additionally, documents were not approved by designated individuals prior to issuance, as demonstrated by the use of an investigation summary form without an approved procedure.

## Related Officers

- [Alicia U. Jacobo](https://www.keypedia.com/people/alicia-u-jacobo/5f75a995-c0df-4615-be88-d401df48ad26)
- [investigator](https://www.keypedia.com/people/susan-m-matthias/cd23c465-4411-4988-8676-2089e265622a)

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