FDA Inspection 937609 — Dujo Logos, Inc. D.B.A. MediComp Medical
The FDA completed an inspection of Dujo Logos, Inc. D.B.A. MediComp Medical on Jun 24, 2015 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
- Jun 24, 2015
- Fiscal Year
- 2015
- Product Type
- Devices
- Project Area
- Compliance: Devices
- Location
- Princeton, MN (United States)