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FDA Inspection
•HyperBranch Medical Technology, Inc.•September 4, 2013

HyperBranch Medical Technology, Inc. – FDA Inspection, Sep 4, 2013

Record Details

This FDA Inspection record concerns HyperBranch Medical Technology, Inc., with an inspection on September 4, 2013, issued by the Center for Devices and Radiological Health, covering devices.

Company
HyperBranch Medical Technology, Inc.
Inspection Date
September 4, 2013
Product Type
Devices
Office
Center for Devices and Radiological Health
View Company Profile

ID · 029aa8e2-2d6f-4bea-8574-67e15261c715

Inspection Facts

Official Action Indicated (OAI)

Significant objectionable conditions were found and regulatory or administrative action is recommended.

Inspection number
847489
FDA center
Medical Devices & Rad Health
Project area
Compliance: Devices

Other FDA inspections of HyperBranch Medical Technology, Inc.

3
DateClassificationOfficeProject area
June 15, 2016NAICenter for Devices and Radiological HealthCompliance: Devices
September 11, 2013VAICenter for Devices and Radiological HealthBioresearch Monitoring
October 23, 2012NAICenter for Devices and Radiological HealthCompliance: Devices
Other documents for HyperBranch Medical Technology, Inc.
  • FDA Inspection 985410 - 2016-06-15
  • FDA Inspection 848517 - 2013-09-11
  • FDA Inspection 804142 - 2012-10-23

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