FDA Inspection 1256781 — Ceribell Inc.

Ceribell Inc. — FEI 3013671918

The FDA completed an inspection of Ceribell Inc. on November 6, 2024 in Sunnyvale, CA. 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
November 6, 2024
Fiscal Year
2025
Product Type
Devices
Project Area
Postmarket Assurance: Devices
Location
Sunnyvale, CA (United States)