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Minnesota MedTec, Inc.

FDA Regulatory Profile

Minnesota MedTec, Inc. has 0 FDA recalls, 5 inspections, 0 510(k) clearances and 0 compliance actions on record.

Latest inspection
Aug 15, 2025 · VAI

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Summary

Record counts and when each FDA source was last refreshed
RecordsCountLast refreshedSource as ofStatus
Recalls0Nov 4, 2026 (checked Nov 8, 2026, unchanged)File dated Nov 3, 2026Current
510(k) clearances0Nov 8, 2026File dated Nov 2, 2026Current
Inspections5Nov 10, 2026Newest record Nov 5, 2026Current
Compliance actions0Nov 2, 2026Newest record Oct 29, 2026Current

Recent FDA Inspections

DateSiteProductClassificationFEI
Aug 15, 2025Maple Grove, MNDevicesVoluntary Action Indicated (VAI)3003007911
Dec 11, 2019Maple Grove, MNDevicesVoluntary Action Indicated (VAI)3003007911
Apr 14, 2016Maple Grove, MNDevicesVoluntary Action Indicated (VAI)3003007911
Jun 11, 2013Maple Grove, MNDevicesNo Action Indicated (NAI)3003007911
Jan 2, 2009Maple Grove, MNDevicesNo Action Indicated (NAI)3003007911

NAI means no objectionable conditions or practices were found during the inspection. VAI means objectionable conditions or practices were found, but the agency is not prepared to take or recommend any administrative or regulatory action. OAI means regulatory and/or administrative actions are recommended.

FDA-Inspected Facilities

FacilityLocationInspectionsLatest
FEI 3003007911Maple Grove, MN5Aug 15, 2025

FDA data resources

Sources: openFDA, FDA Data Dashboard, FDA.gov. Report a data issue: hello@regdatalab.com.