FDA Inspection 895496 — Lumanosity Inc

Lumanosity Inc — FEI 3010152425

The FDA completed an inspection of Lumanosity Inc on Sep 11, 2014 in San Diego, 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
Sep 11, 2014
Fiscal Year
2014
Product Type
Devices
Project Area
Compliance: Devices
Location
San Diego, CA (United States)