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FDA Inspection 952531 — Bard Peripheral Vascular Inc

Bard Peripheral Vascular Inc — FEI 2020394

The FDA completed an inspection of Bard Peripheral Vascular Inc on December 18, 2015 in Tempe, AZ. 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
December 18, 2015
Fiscal Year
2016
Product Type
Devices
Project Area
Postmarket Assurance: Devices
Location
Tempe, AZ (United States)

Facility

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FDA data resources