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FDA Inspection
•Intec Industries Inc•December 13, 2017

Intec Industries Inc – FDA Inspection, Dec 13, 2017

Record Details

This FDA Inspection record concerns Intec Industries Inc, with an inspection on December 13, 2017, issued by the Center for Devices and Radiological Health, covering devices.

Company
Intec Industries Inc
Inspection Date
December 13, 2017
Product Type
Devices
Office
Center for Devices and Radiological Health
Person
  • Wendy R. Blame (Issuing Officer)
View Company Profile

ID · cb8cdb1c-bfcb-4c3c-8f6b-c7e274b7f750

Inspection Facts

No Action Indicated (NAI)

No objectionable conditions or practices were found during the inspection.

Inspection number
1041065
FDA center
Medical Devices & Rad Health
Project area
Postmarket Assurance: Devices

Other FDA inspections of Intec Industries Inc

3
DateClassificationOfficeProject area
March 12, 2015NAICenter for Devices and Radiological HealthCompliance: Devices
February 15, 2012VAICenter for Devices and Radiological HealthCompliance: Devices
August 10, 2010OAICenter for Devices and Radiological HealthCompliance: Devices
Other documents for Intec Industries Inc
  • FDA Inspection 920383 - 2015-03-12
  • FDA Inspection 767114 - 2012-02-15
  • FDA Inspection 674782 - 2010-08-10

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