FDA Inspection 653530 — eScreen Inc

eScreen Inc — FEI 3003110749

The FDA completed an inspection of eScreen Inc on Mar 4, 2010 in Kansas City, MO. 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
Mar 4, 2010
Fiscal Year
2010
Product Type
Devices
Project Area
Compliance: Devices
Location
Kansas City, MO (United States)