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FDA Inspection 833253 — Minnesota MedTec, Inc.

Minnesota MedTec, Inc. — FEI 3003007911

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

Facility

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