FDA Inspection 1068354 — Genprime Inc

Genprime Inc — FEI 3007004742

The FDA completed an inspection of Genprime Inc on Sep 13, 2018 in Spokane, WA. The inspection was classified NAI (No Action Indicated — no objectionable conditions were found). Product area: Devices.

Inspection Details

Classification
No Action Indicated (NAI)
End Date
Sep 13, 2018
Fiscal Year
2018
Product Type
Devices
Project Area
Compliance: Devices
Location
Spokane, WA (United States)