# Bard Peripheral Vascular Inc - Inspection Records

Source: https://www.keypedia.com/companies/bard-peripheral-vascular-inc/1f512f8f-2504-46db-8e99-4719e8970f95

> Inspection records and compliance data for Bard Peripheral Vascular Inc in Tempe, Arizona. 12 FDA inspections on record (1 OAI), last inspected April 21, 2026.

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## Details

- Name: Bard Peripheral Vascular Inc
- FEI Number: 2020394
- Address Line 1: 1625 W 3rd St Bldg 1, 850 W. Rio Salado Prkwy.
- City: Tempe
- State: Arizona
- Zip Code: 85281
- Country Name: United States
- Address: 1625 W 3rd St Bldg 1, 850 W. Rio Salado Prkwy., Tempe, Arizona 85281, United States
- Country: United States

## Related Documents

- FDA Inspection 1313830 - Bard Peripheral Vascular Inc - 2026-04-21 — source: FDA, date: April 21, 2026
- FDA Inspection 1235686 - Bard Peripheral Vascular Inc - 2024-03-08 — classification: No Action Indicated (NAI), source: FDA, date: March 8, 2024
- FDA Inspection 1235686 - Bard Peripheral Vascular Inc - 2024-03-08 — classification: No Action Indicated (NAI), source: FDA, date: March 8, 2024
- FDA Inspection 1076854 - Bard Peripheral Vascular Inc - 2018-11-02 — classification: No Action Indicated (NAI), source: FDA, date: November 2, 2018
- FDA Inspection 1076854 - Bard Peripheral Vascular Inc - 2018-11-02 — classification: No Action Indicated (NAI), source: FDA, date: November 2, 2018
- FDA Inspection 1076854 - Bard Peripheral Vascular Inc - 2018-11-02 — classification: No Action Indicated (NAI), source: FDA, date: November 2, 2018
- FDA Inspection 999931 - Bard Peripheral Vascular Inc - 2017-02-03 — classification: No Action Indicated (NAI), source: FDA, date: February 3, 2017
- FDA Inspection 993498 - Bard Peripheral Vascular Inc - 2016-11-01 — classification: No Action Indicated (NAI), source: FDA, date: November 1, 2016
- FDA Inspection 964385 - Bard Peripheral Vascular Inc - 2016-02-26 — classification: No Action Indicated (NAI), source: FDA, date: February 26, 2016
- FDA Inspection 964385 - Bard Peripheral Vascular Inc - 2016-02-26 — classification: Voluntary Action Indicated (VAI), source: FDA, date: February 26, 2016

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