FDA Inspection 871941 — Dgimed Ortho Inc

Dgimed Ortho Inc — FEI 3007710313

The FDA completed an inspection of Dgimed Ortho Inc on Apr 1, 2014 in Hopkins, 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
Apr 1, 2014
Fiscal Year
2014
Product Type
Devices
Project Area
Compliance: Devices
Location
Hopkins, MN (United States)