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FDA Inspection 1092862 — I-Tek Medical Inc

I-Tek Medical Inc — FEI 3008627763

The FDA completed an inspection of I-Tek Medical Inc on May 30, 2019 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
May 30, 2019
Fiscal Year
2019
Product Type
Devices
Project Area
Radiation Control and Health Safety Act
Location
White Bear Lake, MN (United States)

Facility

Other inspections at this facility

  • 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))
  • 898270 (NAI Tue Sep 30 2014 00:00:00 GMT+0000 (Coordinated Universal Time))

FDA data resources