FDA Inspection 1266300 — Tempus AI, Inc.

Tempus AI, Inc. — FEI 3013200421

The FDA completed an inspection of Tempus AI, Inc. on May 21, 2025 in Chicago, IL. The inspection was classified NAI (No Action Indicated — no objectionable conditions were found). Product area: Devices.

Inspection Details

Classification
No Action Indicated (NAI) (NAI)
End Date
May 21, 2025
Fiscal Year
2025
Product Type
Devices
Project Area
Bioresearch Monitoring
Location
Chicago, IL (United States)

Additional Details

Sponsor, Contract Research Organization