FDA Inspection 985410 — HyperBranch Medical Technology, Inc.

HyperBranch Medical Technology, Inc. — FEI 3005920920

The FDA completed an inspection of HyperBranch Medical Technology, Inc. on June 15, 2016 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
June 15, 2016
Fiscal Year
2016
Product Type
Devices
Project Area
Bioresearch Monitoring
Location
Durham, NC (United States)

Additional Details

Postmarket Audit Inspections