FDA Inspection 833253 — Minnesota MedTec, Inc.
The FDA completed an inspection of Minnesota MedTec, Inc. on Jun 11, 2013 in Maple Grove, 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 11, 2013
- Fiscal Year
- 2013
- Product Type
- Devices
- Project Area
- Postmarket Assurance: Devices
- Location
- Maple Grove, MN (United States)