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FDA Inspection 804142 — HyperBranch Medical Technology, Inc.

HyperBranch Medical Technology, Inc. — FEI 3005920920

The FDA completed an inspection of HyperBranch Medical Technology, Inc. on October 23, 2012 in Durham, NC. The inspection was classified NAI (No Action Indicated — no objectionable conditions were found). Product area: Devices.

Inspection Details

Classification
No Action Indicated (NAI) (NAI)
End Date
October 23, 2012
Fiscal Year
2013
Product Type
Devices
Project Area
Compliance: Devices
Location
Durham, NC (United States)

Facility

Other inspections at this facility

  • 985410 (NAI Wed Jun 15 2016 00:00:00 GMT+0000 (Coordinated Universal Time))
  • 848517 (VAI Wed Sep 11 2013 00:00:00 GMT+0000 (Coordinated Universal Time))
  • 847489 (OAI Wed Sep 04 2013 00:00:00 GMT+0000 (Coordinated Universal Time))

FDA data resources