FDA Inspection
Minnesota MedTec, Inc.Minnesota MedTec, Inc. – FDA Inspection, Apr 14, 2016
Record Details
This FDA Inspection record concerns Minnesota MedTec, Inc., with an inspection on April 14, 2016, issued by the Center for Devices and Radiological Health, covering devices.
- Company
- Minnesota MedTec, Inc.
- Inspection Date
- April 14, 2016
- Product Type
- Devices
View Company Profile
ID · af2382ff-2dde-4700-a3bb-dd15ede250dc
Inspection Facts
Voluntary Action Indicated (VAI)
Objectionable conditions were found, but FDA is not prepared to take or recommend regulatory action.
- Inspection number
- 972365
- FDA center
- Medical Devices & Rad Health
- Project area
- Compliance: Devices
FDA Citations
1- 21 CFR 820.100(a)Lack of or inadequate procedures
Full citation text and observation details available on the Dashboard.
Other FDA inspections of Minnesota MedTec, Inc.
4| Date | Classification | Office | Project area |
|---|---|---|---|
| August 15, 2025 | NAI | Minneapolis District Office | Postmarket Assurance: Medical Devices |
| December 11, 2019 | VAI | Center for Devices and Radiological Health | Compliance: Devices |
| June 11, 2013 | NAI | Center for Devices and Radiological Health | Postmarket Assurance: Devices |
| January 2, 2009 | NAI | Center for Devices and Radiological Health | Compliance: Devices |
Other documents for Minnesota MedTec, Inc.
- FDA Inspection 1279944 - 2025-08-15
- FDA Inspection 1112375 - 2019-12-11
- FDA Inspection 833253 - 2013-06-11
- FDA Inspection 557284 - 2009-01-02
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