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FDA Inspection
•HyperBranch Medical Technology, Inc.•June 15, 2016

HyperBranch Medical Technology, Inc. – FDA Inspection, Jun 15, 2016

Record Details

This FDA Inspection record concerns HyperBranch Medical Technology, Inc., with an inspection on June 15, 2016, issued by the Center for Devices and Radiological Health, covering devices.

Company
HyperBranch Medical Technology, Inc.
Inspection Date
June 15, 2016
Product Type
Devices
Office
Center for Devices and Radiological Health
View Company Profile

ID · a0133b51-fb68-4a8c-a5e4-a27b5d09d4b1

Inspection Facts

No Action Indicated (NAI)

No objectionable conditions or practices were found during the inspection.

Inspection number
985410
FDA center
Medical Devices & Rad Health
Project area
Compliance: Devices

Other FDA inspections of HyperBranch Medical Technology, Inc.

3
DateClassificationOfficeProject area
September 11, 2013VAICenter for Devices and Radiological HealthBioresearch Monitoring
September 4, 2013OAICenter for Devices and Radiological HealthCompliance: Devices
October 23, 2012NAICenter for Devices and Radiological HealthCompliance: Devices
Other documents for HyperBranch Medical Technology, Inc.
  • FDA Inspection 848517 - 2013-09-11
  • FDA Inspection 847489 - 2013-09-04
  • FDA Inspection 804142 - 2012-10-23

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