# FDA Inspection 1097098 - Ceribell Inc. - June 25, 2019

Source: https://www.keypedia.com/records/fda_inspections/ceribell-inc/3cf04eef-bb76-4cb0-bc05-194e2b6fc090
Source feed: FDA_Inspections

> FDA Inspection 1097098 for Ceribell Inc. on June 25, 2019. Classification: No Action Indicated (NAI).

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## Details

- Record Type: FDA Inspection
- Inspection ID: 1097098
- Company Name: Ceribell Inc.
- Inspection Date: 2019-06-25
- Classification: No Action Indicated (NAI)
- Project Area: Compliance: Devices
- Product Type: Devices
- Office Name: Center for Devices and Radiological Health

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Company: https://www.keypedia.com/companies/ceribell-inc/14bac3ec-5365-4fbd-8090-8ee9f101e7e2

Office: https://www.keypedia.com/offices/center-for-devices-and-radiological-health/9d89aff6-e435-4764-87be-f58c01aca7f7