FDA Inspection 635483 — MEDTRONIC IRELAND

MEDTRONIC IRELAND — FEI 3002806434

The FDA completed an inspection of MEDTRONIC IRELAND on December 10, 2009 in Galway. The inspection was classified NAI (No Action Indicated — no objectionable conditions were found). Product area: Devices.

Inspection Details

Classification
No Action Indicated (NAI) (NAI)
End Date
December 10, 2009
Fiscal Year
2010
Product Type
Devices
Project Area
Compliance: Devices
Location
Galway (Ireland)