FDA Inspection 1050339 — Sooka Inc

Sooka Inc — FEI 3007671445

The FDA completed an inspection of Sooka Inc on Feb 14, 2018 in boca raton, FL. 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
Feb 14, 2018
Fiscal Year
2018
Product Type
Devices
Project Area
Postmarket Assurance: Devices
Location
boca raton, FL (United States)