FDA inspection

Medtox Laboratories, Inc.: FDA inspection ending Jun 28, 2005

FDA inspection 385209 · Voluntary Action Indicated (VAI) · Saint Paul, MN

Key facts

Inspection ID 385209
Firm Medtox Laboratories, Inc.
FEI number 3001239310
Address 402 County Road D W
City Saint Paul
State MN
ZIP 55112-3522
Fiscal year 2005
Inspection end date Jun 28, 2005
Classification Voluntary Action Indicated (VAI)
Project area Bio-Research Monit: Human Drugs
Product type Drugs

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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