Minnetronix, Inc.

Form 483

Saint Paul, MinnesotaFEI 3000203066Issued April 01, 2026

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 3000203066.

Observations2

Issue DateApril 01, 2026

StatusNo Warning Letter

Related Inspections5

Establishment Details

Firm: Minnetronix, Inc.
Location: Saint Paul, Minnesota
FEI Number: 3000203066
Product Type: Devices
Issue Date: April 01, 2026
Country: United States

Inspection History, 2017 to 2026

NAI4

VAI1

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

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Minnetronix, Inc. FDA Form 483, Saint Paul, Minnesota, April 1, 2026