FDA Inspection 1267055 — Innovize LLC

Innovize LLC — FEI 3007867940

The FDA completed an inspection of Innovize LLC on March 26, 2025 in Saint Paul, MN. The inspection was classified NAI (No Action Indicated — no objectionable conditions were found). 2 citations were issued during this inspection. Product area: Devices.

Inspection Details

Classification
No Action Indicated (NAI) (NAI)
End Date
March 26, 2025
Fiscal Year
2025
Product Type
Devices
Project Area
Postmarket Assurance: Devices
Location
Saint Paul, MN (United States)

Citations

IDCFRDescription
337521 CFR 820.198(e)Records of complaint investigation
45421 CFR 820.40(a)Document review, approval by designated individual