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FDA Inspection
•ITG Int.•October 20, 2017

ITG Int. – FDA Inspection, Oct 20, 2017

Record Details

This FDA Inspection record concerns ITG Int., with an inspection on October 20, 2017, issued by the Center for Devices and Radiological Health, covering devices.

Company
ITG Int.
Inspection Date
October 20, 2017
Product Type
Devices
Office
Center for Devices and Radiological Health
Person
  • Teresa K. Kastner
View Company Profile

ID · 6a0c4907-0339-4613-a060-d84d53af3e4c

Inspection Facts

No Action Indicated (NAI)

No objectionable conditions or practices were found during the inspection.

Inspection number
1031096
FDA center
Medical Devices & Rad Health
Project area
Postmarket Assurance: Devices

Other FDA inspections of ITG Int.

1
DateClassificationOfficeProject area
August 31, 2022NAICenter for Devices and Radiological HealthCompliance: Devices
Other documents for ITG Int.
  • FDA Inspection 1179502 - 2022-08-31

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