# Medtronic Vascular, Inc., Santa Rosa, CA – FDA Inspections

Source: https://www.keypedia.com/companies/medtronic-vascular-inc/3f4db393-29fc-4eec-91ae-845a424fe407

> Inspection records and compliance data for Medtronic Vascular, Inc. in Santa Rosa, California. 10 FDA inspections on record, last inspected July 11, 2019.

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## Details

- Name: Medtronic Vascular, Inc.
- FEI Number: 3001452571
- Address Line 1: 3576 Unocal Pl
- City: Santa Rosa
- State: California
- Zip Code: 95403
- Country Name: United States
- Address: 3576 Unocal Pl, Santa Rosa, California 95403, United States
- Country: United States

## Related Documents

- FDA Inspection 1096966 - Medtronic Vascular, Inc. - 2019-07-11 — classification: No Action Indicated (NAI), source: FDA, date: July 11, 2019
- FDA Inspection 1096966 - Medtronic Vascular, Inc. - 2019-07-11 — classification: No Action Indicated (NAI), source: FDA, date: July 11, 2019
- FDA Inspection 1096966 - Medtronic Vascular, Inc. - 2019-07-11 — classification: No Action Indicated (NAI), source: FDA, date: July 11, 2019
- FDA Inspection 1030899 - Medtronic Vascular, Inc. - 2017-08-31 — classification: No Action Indicated (NAI), source: FDA, date: August 31, 2017
- FDA Inspection 901694 - Medtronic Vascular, Inc. - 2014-11-07 — classification: No Action Indicated (NAI), source: FDA, date: November 7, 2014
- FDA Inspection 901694 - Medtronic Vascular, Inc. - 2014-11-07 — classification: No Action Indicated (NAI), source: FDA, date: November 7, 2014
- FDA Inspection 901694 - Medtronic Vascular, Inc. - 2014-11-07 — classification: No Action Indicated (NAI), source: FDA, date: November 7, 2014
- FDA Inspection 855281 - Medtronic Vascular, Inc. - 2013-11-14 — classification: No Action Indicated (NAI), source: FDA, date: November 14, 2013
- FDA Inspection 855281 - Medtronic Vascular, Inc. - 2013-11-14 — classification: No Action Indicated (NAI), source: FDA, date: November 14, 2013
- FDA Inspection 819376 - Medtronic Vascular, Inc. - 2013-02-22 — classification: No Action Indicated (NAI), source: FDA, date: February 22, 2013

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