FDA Inspection
HyperBranch Medical Technology, Inc.HyperBranch Medical Technology, Inc. – FDA Inspection, Sep 11, 2013
Record Details
This FDA Inspection record concerns HyperBranch Medical Technology, Inc., with an inspection on September 11, 2013, issued by the Center for Devices and Radiological Health, covering devices.
- Inspection Date
- September 11, 2013
- Product Type
- Devices
View Company Profile
ID · 0e0414a9-cf75-4066-9929-c94f29e57b7b
Inspection Facts
Voluntary Action Indicated (VAI)
Objectionable conditions were found, but FDA is not prepared to take or recommend regulatory action.
- Inspection number
- 848517
- FDA center
- Medical Devices & Rad Health
- Project area
- Bioresearch Monitoring
Other FDA inspections of HyperBranch Medical Technology, Inc.
3| Date | Classification | Office | Project area |
|---|---|---|---|
| June 15, 2016 | NAI | Center for Devices and Radiological Health | Compliance: Devices |
| September 4, 2013 | OAI | Center for Devices and Radiological Health | Compliance: Devices |
| October 23, 2012 | NAI | Center for Devices and Radiological Health | Compliance: Devices |
Other documents for HyperBranch Medical Technology, Inc.
- FDA Inspection 985410 - 2016-06-15
- FDA Inspection 847489 - 2013-09-04
- FDA Inspection 804142 - 2012-10-23
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