FDA Inspection 664298 — EasyDx Inc.

EasyDx Inc. — FEI 1000115726

The FDA completed an inspection of EasyDx Inc. on May 27, 2010 in Roseville, MN. 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
May 27, 2010
Fiscal Year
2010
Product Type
Devices
Project Area
Compliance: Devices
Location
Roseville, MN (United States)