Home / Inspections / 1211561

FDA Inspection 1211561 — Arrow International, Inc. (Subsidiary of Teleflex, Inc.)

Arrow International, Inc. (Subsidiary of Teleflex, Inc.) — FEI 3015859709

The FDA completed an inspection of Arrow International, Inc. (Subsidiary of Teleflex, Inc.) on July 14, 2023 in Wyomissing, PA. The inspection was classified NAI (No Action Indicated — no objectionable conditions were found). Product area: Devices.

Inspection Details

Classification
No Action Indicated (NAI) (NAI)
End Date
July 14, 2023
Fiscal Year
2023
Product Type
Devices
Project Area
Compliance: Devices
Location
Wyomissing, PA (United States)

Facility

Other inspections at this facility

  • 977560 (VAI Mon Jun 20 2016 00:00:00 GMT+0000 (Coordinated Universal Time))
  • 897017 (VAI Wed Sep 24 2014 00:00:00 GMT+0000 (Coordinated Universal Time))
  • 859917 (NAI Wed Dec 18 2013 00:00:00 GMT+0000 (Coordinated Universal Time))
  • 635947 (VAI Fri Dec 18 2009 00:00:00 GMT+0000 (Coordinated Universal Time))

FDA data resources