# FDA Inspection 595178 - Medtronic Vascular, Inc. - June 19, 2009

Source: https://www.keypedia.com/records/fda_inspections/medtronic-vascular-inc/6121ddf3-8cb8-4ff9-913a-e7eba8070942
Source feed: FDA_Inspections

> FDA Inspection 595178 for Medtronic Vascular, Inc. on June 19, 2009. Classification: No Action Indicated (NAI).

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## Details

- Record Type: FDA Inspection
- Inspection ID: 595178
- Company Name: Medtronic Vascular, Inc.
- Inspection Date: 2009-06-19
- Classification: No Action Indicated (NAI)
- Project Area: Postmarket Assurance: Devices
- Product Type: Devices
- Office Name: Center for Devices and Radiological Health

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Company: https://www.keypedia.com/companies/medtronic-vascular-inc/9ea1f72c-f6bc-46cb-984b-0272e05bf68a

Office: https://www.keypedia.com/offices/center-for-devices-and-radiological-health/9d89aff6-e435-4764-87be-f58c01aca7f7