FDA inspection

Minnesota MedTec, Inc.: FDA inspection ending Jun 11, 2013

FDA inspection 833253 · No Action Indicated (NAI) · Maple Grove, MN

Key facts

Inspection ID 833253
Firm Minnesota MedTec, Inc.
FEI number 3003007911
Address 11760 Justen Cir Ste B
City Maple Grove
State MN
ZIP 55369
Country United States
Fiscal year 2013
Inspection end date Jun 11, 2013
Classification No Action Indicated (NAI)
Project area Compliance: Devices
Product type Devices

At a glance

  • None Citations
  • None Posted citations
  • No Warning letter followed
  • No 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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