FDA Inspection 1256781 — Ceribell Inc.

Ceribell Inc. — FEI 3013671918

The FDA completed an inspection of Ceribell Inc. on Nov 6, 2024 in Sunnyvale, CA. The inspection was classified NAI (No Action Indicated — no objectionable conditions or practices were found during the inspection). Product area: Devices.

Inspection details

Classification
No Action Indicated (NAI)
End Date
Nov 6, 2024
Fiscal Year
2025
Product Type
Devices
Project Area
Compliance: Devices
Location
Sunnyvale, CA (United States)

Sources: openFDA, FDA Data Dashboard, FDA.gov. Report a data issue: hello@regdatalab.com.