FDA inspection

Minnesota MedTec, Inc.: FDA inspection ending Aug 3, 2002

FDA inspection 237196 · Voluntary Action Indicated (VAI) · Maple Grove, MN

Key facts

Inspection ID 237196
Firm Minnesota MedTec, Inc.
FEI number 3003007911
Address 11760 Justen Cir Ste B
City Maple Grove
State MN
ZIP 55369-9256
Fiscal year 2002
Inspection end date Aug 3, 2002
Classification Voluntary Action Indicated (VAI)
Project area Compliance: Med Devices
Product type Devices

At a glance

  • None Citations
  • 1–9 Posted citations
  • No Warning letter followed
  • Yes Form FDA 483 issued
  • No Establishment inspection report (EIR) exists
  • 1–9 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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