FDA Inspection 647582 — Dujo Logos, Inc. D.B.A. MediComp Medical

Dujo Logos, Inc. D.B.A. MediComp Medical — FEI 2183585

The FDA completed an inspection of Dujo Logos, Inc. D.B.A. MediComp Medical on Feb 22, 2010 in Princeton, 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
Feb 22, 2010
Fiscal Year
2010
Product Type
Devices
Project Area
Compliance: Devices
Location
Princeton, MN (United States)