FDA Inspection 1038139 — Dujo Logos, Inc. D.B.A. MediComp Medical
The FDA completed an inspection of Dujo Logos, Inc. D.B.A. MediComp Medical on Jan 4, 2018 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
- Jan 4, 2018
- Fiscal Year
- 2018
- Product Type
- Devices
- Project Area
- Postmarket Assurance: Devices
- Location
- Princeton, MN (United States)