# HyperBranch Medical Technology, Inc. – FDA Inspection, Sep 11, 2013

Source: https://www.keypedia.com/records/fda_inspections/hyperbranch-medical-technology-inc/0e0414a9-cf75-4066-9929-c94f29e57b7b
Source feed: FDA_Inspections

> FDA inspection 848517 of HyperBranch Medical Technology, Inc., September 11, 2013. Classification: Voluntary Action Indicated (VAI). 3 other FDA inspections on record for this company.

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## Details

- Record Type: FDA Inspection
- Inspection ID: 848517
- Company Name: HyperBranch Medical Technology, Inc.
- Inspection Date: 2013-09-11
- Classification: Voluntary Action Indicated (VAI)
- Classification Code: VAI
- Project Area: Bioresearch Monitoring
- Product Type: Devices
- Center: Medical Devices & Rad Health
- Office Name: Center for Devices and Radiological Health
- Citation Count: 0

## Related Documents

- [FDA Inspection 985410 - 2016-06-15](https://www.keypedia.com/records/fda_inspections/hyperbranch-medical-technology-inc/a0133b51-fb68-4a8c-a5e4-a27b5d09d4b1)
- [FDA Inspection 847489 - 2013-09-04](https://www.keypedia.com/records/fda_inspections/hyperbranch-medical-technology-inc/029aa8e2-2d6f-4bea-8574-67e15261c715)
- FDA Inspection 804142 - 2012-10-23

Company: https://www.keypedia.com/companies/hyperbranch-medical-technology-inc/94fde96c-fa9f-46d1-92b4-ed5947418a5c

Office: https://www.keypedia.com/offices/center-for-devices-and-radiological-health/9d89aff6-e435-4764-87be-f58c01aca7f7