FDA inspection

Arrow International, Inc. (Subsidiary of Teleflex, Inc.): FDA inspection ending Jul 14, 2023

FDA inspection 1211561 · No Action Indicated (NAI) · Wyomissing, PA

Key facts

Inspection ID 1211561
Firm Arrow International, Inc. (Subsidiary of Teleflex, Inc.)
FEI number 3015859709
Address 35 Innovation Way
City Wyomissing
State PA
ZIP 19610
Country United States
Fiscal year 2023
Inspection end date Jul 14, 2023
Classification No Action Indicated (NAI)
Project area Compliance: Devices
Product type Devices

At a glance

  • None Citations
  • None Posted citations
  • No Warning letter followed
  • No 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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