FDA inspection

Arrow International, Inc. (Subsidiary of Teleflex, Inc.): FDA inspection ending Dec 18, 2009

FDA inspection 635947 · Voluntary Action Indicated (VAI) · Wyomissing, PA

Key facts

Inspection ID 635947
Firm Arrow International, Inc. (Subsidiary of Teleflex, Inc.)
FEI number 3015859709
Address 2400 Bernville Road
City Wyomissing
State PA
ZIP 19610
Country United States
Fiscal year 2010
Inspection end date Dec 18, 2009
Classification Voluntary Action Indicated (VAI)
Project area Compliance: Devices
Product type Devices

At a glance

  • 1–9 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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