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FDA Inspection 898270 — I-Tek Medical Inc

I-Tek Medical Inc — FEI 3008627763

The FDA completed an inspection of I-Tek Medical Inc on September 30, 2014 in White Bear Lake, MN. 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
September 30, 2014
Fiscal Year
2014
Product Type
Devices
Project Area
Compliance: Devices
Location
White Bear Lake, MN (United States)

Facility

Other inspections at this facility

  • 1092862 (NAI Thu May 30 2019 00:00:00 GMT+0000 (Coordinated Universal Time))
  • 988503 (NAI Mon Sep 26 2016 00:00:00 GMT+0000 (Coordinated Universal Time))
  • 910481 (NAI Thu Nov 20 2014 00:00:00 GMT+0000 (Coordinated Universal Time))

FDA data resources