FDA inspection

Medtox Diagnostics, Inc.: FDA inspection ending Mar 30, 2017

FDA inspection 1009293 · No Action Indicated (NAI) · Burlington, NC

Key facts

Inspection ID 1009293
Firm Medtox Diagnostics, Inc.
FEI number 3004175381
Address 1640 Nova Ln
City Burlington
State NC
ZIP 27215
Country United States
Fiscal year 2017
Inspection end date Mar 30, 2017
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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