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FDA Inspection
•I-Tek Medical Inc•May 30, 2019

I-Tek Medical Inc – FDA Inspection, May 30, 2019

Record Details

This FDA Inspection record concerns I-Tek Medical Inc, with an inspection on May 30, 2019, issued by the Center for Devices and Radiological Health, covering devices.

Company
I-Tek Medical Inc
Inspection Date
May 30, 2019
Product Type
Devices
Office
Center for Devices and Radiological Health
Person
  • Jennifer S. Ness (Company Rep)
View Company Profile

ID · 51d572dc-6192-49d7-840c-ca108da6af71

Inspection Facts

No Action Indicated (NAI)

No objectionable conditions or practices were found during the inspection.

Inspection number
1092862
FDA center
Medical Devices & Rad Health
Project area
Radiation Control and Health Safety Act

Other FDA inspections of I-Tek Medical Inc

3
DateClassificationOfficeProject area
September 26, 2016NAICenter for Devices and Radiological HealthCompliance: Devices
November 20, 2014NAICenter for Devices and Radiological HealthCompliance: Devices
September 30, 2014NAICenter for Devices and Radiological HealthCompliance: Devices
Other documents for I-Tek Medical Inc
  • FDA Inspection 988503 - 2016-09-26
  • FDA Inspection 910481 - 2014-11-20
  • FDA Inspection 898270 - 2014-09-30

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