Minnesota MedTec, Inc.August 15, 2025

FDA 483 - Minnesota MedTec, Inc. - August 15, 2025

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Minnesota Medtec, Inc., a contract manufacturer in Maple Grove, MN, received a Form FDA-483 citing two observations related to its quality system. The inspection revealed deficiencies in establishing adequate procedures for personnel training and ensuring that all purchased products and services conform to specified requirements. Specifically, the firm failed to train key personnel according to its SOPs and did not properly approve critical suppliers.

Company: Minnesota MedTec, Inc.
Inspection Date: August 15, 2025
Product Type: Device
Office: Minneapolis District Office
Person: Alicia U. Jacobo

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