FDA Inspection 1172530 — Dujo Logos, Inc. D.B.A. MediComp Medical
The FDA completed an inspection of Dujo Logos, Inc. D.B.A. MediComp Medical on Jun 2, 2022 in Princeton, MN. The inspection was classified VAI (Voluntary Action Indicated — objectionable conditions or practices were found, but the agency is not prepared to take or recommend any administrative or regulatory action). 4 citations were issued during this inspection. Product area: Devices.
Inspection Details
- Classification
- Voluntary Action Indicated (VAI)
- End Date
- Jun 2, 2022
- Fiscal Year
- 2022
- Product Type
- Devices
- Project Area
- Compliance: Devices
- Location
- Princeton, MN (United States)
Citations
| ID | CFR | Description |
|---|---|---|
| 14713 | 21 CFR 820.198(a) | Lack of or inadequate complaint procedures |
| 14721 | 21 CFR 820.70(g)(2) | Periodic equipment inspections |
| 14722 | 21 CFR 820.40 | Procedures not adequately established or maintained |
| 479 | 21 CFR 820.50 | Purchasing controls, Lack of or inadequate procedures |