FDA inspection

Accogent Pausch: FDA inspection ending Apr 18, 2005

FDA inspection 375033 · Voluntary Action Indicated (VAI) · Tinton Falls, NJ

Key facts

Inspection ID 375033
Firm Accogent Pausch
FEI number 2243057
Address 808 Shrewsbury Ave
City Tinton Falls
State NJ
ZIP 07724-3002
Fiscal year 2005
Inspection end date Apr 18, 2005
Classification Voluntary Action Indicated (VAI)
Project area Compliance: Med Devices
Product type Devices

At a glance

  • None Citations
  • 1–9 Posted citations
  • No Warning letter followed
  • Yes Form FDA 483 issued
  • No 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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