FDA inspection

HyperBranch Medical Technology, Inc.: FDA inspection ending Sep 11, 2013

FDA inspection 848517 · Voluntary Action Indicated (VAI) · Durham, NC

Key facts

Inspection ID 848517
Firm HyperBranch Medical Technology, Inc.
FEI number 3005920920
Address 800 Capitola Dr Ste 12
City Durham
State NC
ZIP 27713
Country United States
Fiscal year 2013
Inspection end date Sep 11, 2013
Classification Voluntary Action Indicated (VAI)
Project area Bioresearch Monitoring
Product type Devices

At a glance

  • None Citations
  • 1–9 Posted citations
  • No Warning letter followed
  • Yes Form FDA 483 issued
  • Yes Establishment inspection report (EIR) exists
  • 1–9 Inspections at this FEI

Counts are shown as ranges. Exact figures, trends and every underlying record are available in Orca1.

About FDA inspections

FDA inspections are classified as No Action Indicated (NAI), Voluntary Action Indicated (VAI) or Official Action Indicated (OAI). Inspections of individual clinical investigators are not published here.

Source: U.S. Food and Drug Administration (FDA), inspection classification data

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