FDA Inspection 1239271 — Akili Interactive Labs, Inc.

Akili Interactive Labs, Inc. — FEI 3013341423

The FDA completed an inspection of Akili Interactive Labs, Inc. on May 23, 2024 in Kirkland, WA. The inspection was classified NAI (No Action Indicated — no objectionable conditions were found). 2 citations were issued during this inspection. Product area: Devices.

Inspection Details

Classification
No Action Indicated (NAI) (NAI)
End Date
May 23, 2024
Fiscal Year
2024
Product Type
Devices
Project Area
Postmarket Assurance: Devices
Location
Kirkland, WA (United States)

Citations

IDCFRDescription
1471321 CFR 820.198(a)Lack of or inadequate complaint procedures
313021 CFR 820.100(a)Lack of or inadequate procedures