# FDA Inspection 880677 - Medtronic Vascular Galway DBA Medtronic Ireland - May 15, 2014

Source: https://www.keypedia.com/records/fda_inspections/medtronic-vascular-galway-dba-medtronic-ireland/e2c26fc8-d381-4ade-9e65-449d50f8bc12
Source feed: FDA_Inspections

> FDA Inspection 880677 for Medtronic Vascular Galway DBA Medtronic Ireland on May 15, 2014. Classification: No Action Indicated (NAI).

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## Details

- Record Type: FDA Inspection
- Inspection ID: 880677
- Company Name: Medtronic Vascular Galway DBA Medtronic Ireland
- Inspection Date: 2014-05-15
- Classification: No Action Indicated (NAI)
- Project Area: Compliance: Devices
- Product Type: Devices
- Office Name: Center for Devices and Radiological Health

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Company: https://www.keypedia.com/companies/medtronic-vascular-galway-dba-medtronic-ireland/eb59435f-e3d7-493a-9b22-52e3575f021d

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