FDA inspection

Minnetronix, Inc.: FDA inspection ending Jun 4, 2025

FDA inspection 1272311 · No Action Indicated (NAI) · Saint Paul, MN

Key facts

Inspection ID 1272311
Firm Minnetronix, Inc.
FEI number 3000203066
Address 1635 Energy Park Dr
City Saint Paul
State MN
ZIP 55108-2703
Fiscal year 2025
Inspection end date Jun 4, 2025
Classification No Action Indicated (NAI)
Project area Product Evaluation: Medical Devices
Product type Devices

At a glance

  • None Citations
  • None Posted citations
  • No Warning letter followed
  • Yes Form FDA 483 issued
  • No Establishment inspection report (EIR) exists
  • 10–99 Inspections at this FEI

Counts are shown as ranges. Exact figures, trends and every underlying record are available in Orca1.

About FDA inspections

FDA inspections are classified as No Action Indicated (NAI), Voluntary Action Indicated (VAI) or Official Action Indicated (OAI). Inspections of individual clinical investigators are not published here.

Source: U.S. Food and Drug Administration (FDA), inspection classification data

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