FDA Inspection 1097306 — Cogstate Inc.

Cogstate Inc. — FEI 3014109815

The FDA completed an inspection of Cogstate Inc. on July 24, 2019 in New Haven, CT. The inspection was classified VAI (Voluntary Action Indicated — objectionable conditions were found but do not meet the threshold for regulatory action). 2 citations were issued during this inspection. Product area: Devices.

Inspection Details

Classification
Voluntary Action Indicated (VAI) (VAI)
End Date
July 24, 2019
Fiscal Year
2019
Product Type
Devices
Project Area
Compliance: Devices
Location
New Haven, CT (United States)

Citations

IDCFRDescription
232721 CFR 820.22Quality audits - Lack of or inadequate procedures
366921 CFR 820.20(c)Management review - defined interval, sufficient frequency