Minnesota MedTec, Inc.

Form 483FOIA Uncovered

Maple Grove, Minnesota, United StatesFEI 3003007911Issued December 11, 2019

View FDA's Record for This Firm

Source: FDA inspection record. Confirmed against FDA's published inspection data for this establishment and inspection date. FDA has published the inspection and what it cited, but not the form itself, which usually takes six to twelve months. To check it, open FDA's record for this establishment on FDA's Data Dashboard, listed under FEI 3003007911.

Observations3

Issue DateDecember 11, 2019

StatusNo Warning Letter

Related Inspections5

Establishment Details

Firm: Minnesota MedTec, Inc.
Location: Maple Grove, Minnesota, United States
FEI Number: 3003007911
Product Type: Devices
Issue Date: December 11, 2019
Country: United States

Inspection History, 2009 to 2025

NAI2

VAI3

NAI means No Action Indicated. VAI means Voluntary Action Indicated.

Act on This Form 483

FDA Inspection ReadinessSee how your operations would hold up to the same scrutiny.CAPA & InvestigationsScore how you would investigate and close findings like these.Talk to a SpecialistWalk through these observations with a ComplianceQuest expert.

Minnesota MedTec, Inc. FDA Form 483, Maple Grove, Minnesota, December 11, 2019