FDA Inspection 1009293 — Medtox Diagnostics, Inc.

Medtox Diagnostics, Inc. — FEI 3004175381

The FDA completed an inspection of Medtox Diagnostics, Inc. on March 30, 2017 in Burlington, NC. The inspection was classified NAI (No Action Indicated — no objectionable conditions were found). Product area: Devices.

Inspection Details

Classification
No Action Indicated (NAI) (NAI)
End Date
March 30, 2017
Fiscal Year
2017
Product Type
Devices
Project Area
Compliance: Devices
Location
Burlington, NC (United States)