FDA inspection

Arrow International, Inc. (subsidiary of Teleflex, Inc.): FDA inspection ending Oct 16, 2003

FDA inspection 296583 · No Action Indicated (NAI) · Chelmsford, MA

Key facts

Inspection ID 296583
Firm Arrow International, Inc. (subsidiary of Teleflex, Inc.)
FEI number 3010532612
Address 16 Elizabeth Dr
City Chelmsford
State MA
ZIP 01824-4112
Fiscal year 2004
Inspection end date Oct 16, 2003
Classification No Action Indicated (NAI)
Project area Compliance: Med Devices
Product type Devices

At a glance

  • None Citations
  • None Posted citations
  • No Warning letter followed
  • Yes Form FDA 483 issued
  • No Establishment inspection report (EIR) exists
  • 10–99 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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