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FDA Inspection 897017 — 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 September 24, 2014 in Wyomissing, PA. The inspection was classified VAI (Voluntary Action Indicated — objectionable conditions were found but do not meet the threshold for regulatory action). Product area: Devices.

Inspection Details

Classification
Voluntary Action Indicated (VAI) (VAI)
End Date
September 24, 2014
Fiscal Year
2014
Product Type
Devices
Project Area
Postmarket Assurance: Devices
Location
Wyomissing, PA (United States)

Facility

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FDA data resources