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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
Bioresearch Monitoring
Location
Tempe, AZ (United States)

Additional Details

Postmarket Audit Inspections

Facility

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Recent compliance actions

FDA data resources