Arrow International, Inc. (Subsidiary of Teleflex, Inc.)

Form 483

Wyomissing, Pennsylvania, United StatesFEI 3015859709Issued June 20, 2016

View FDA's Record for This Firm

Source: FDA inspection record. Confirmed against FDA's published inspection data for this establishment and inspection date. FDA has published the inspection and what it cited, but not the form itself, which usually takes six to twelve months. To check it, open FDA's record for this establishment on FDA's Data Dashboard, listed under FEI 3015859709.

Observations1

Issue DateJune 20, 2016

StatusNo Warning Letter

Related Inspections5

Establishment Details

Firm: Arrow International, Inc. (Subsidiary of Teleflex, Inc.)
Location: Wyomissing, Pennsylvania, United States
FEI Number: 3015859709
Product Type: Devices
Issue Date: June 20, 2016
Country: United States

Inspection History, 2009 to 2023

NAI2

VAI3

NAI means No Action Indicated. VAI means Voluntary Action Indicated.

Act on This Form 483

FDA Inspection ReadinessSee how your operations would hold up to the same scrutiny.CAPA & InvestigationsScore how you would investigate and close findings like these.Talk to a SpecialistWalk through these observations with a ComplianceQuest expert.

Arrow International, Inc. (Subsidiary of Teleflex, Inc.) FDA Form 483, Wyomissing, Pennsylvania, June 20, 2016