FDA Inspection 847489 — HyperBranch Medical Technology, Inc.

HyperBranch Medical Technology, Inc. — FEI 3005920920

The FDA completed an inspection of HyperBranch Medical Technology, Inc. on September 4, 2013 in Durham, NC. The inspection was classified OAI (Official Action Indicated — objectionable conditions were found and regulatory action is recommended). Product area: Devices.

Inspection Details

Classification
Official Action Indicated (OAI) (OAI)
End Date
September 4, 2013
Fiscal Year
2013
Product Type
Devices
Project Area
Compliance: Devices
Location
Durham, NC (United States)