FDA inspection

Minnetronix, Inc.: FDA inspection ending Apr 1, 2026

FDA inspection 1310502 · Voluntary Action Indicated (VAI) · Saint Paul, Minnesota

Key facts

Inspection ID 1310502
Firm Minnetronix, Inc.
FEI number 3000203066
Address 1635 Energy Park Dr
City Saint Paul
State Minnesota
ZIP 55108
Fiscal year 2026
Inspection end date Apr 1, 2026
Classification Voluntary Action Indicated (VAI)
Project area Project Evaluation: Devices
Product type Devices

At a glance

  • 1–9 Citations
  • 1–9 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

Browse all FDA inspections