FDA Inspection 1076647 — Brain Sentinel, Inc.

Brain Sentinel, Inc. — FEI 3012995918

The FDA completed an inspection of Brain Sentinel, Inc. on Nov 28, 2018 in San Antonio, TX. 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 28, 2018
Fiscal Year
2019
Product Type
Devices
Project Area
Postmarket Assurance: Devices
Location
San Antonio, TX (United States)

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