FDA Inspection 557284 — Minnesota MedTec, Inc.
The FDA completed an inspection of Minnesota MedTec, Inc. on January 2, 2009 in Maple Grove, MN. The inspection was classified NAI (No Action Indicated — no objectionable conditions were found). Product area: Devices.
Inspection Details
- Classification
- No Action Indicated (NAI) (NAI)
- End Date
- January 2, 2009
- Fiscal Year
- 2009
- Product Type
- Devices
- Project Area
- Compliance: Devices
- Location
- Maple Grove, MN (United States)