FDA Inspection 732055 — MEDTRONIC IRELAND

MEDTRONIC IRELAND — FEI 3002806434

The FDA completed an inspection of MEDTRONIC IRELAND on May 26, 2011 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
May 26, 2011
Fiscal Year
2011
Product Type
Devices
Project Area
Postmarket Assurance: Devices
Location
Galway (Ireland)