FDA Inspection 823591 — MEDTRONIC IRELAND

MEDTRONIC IRELAND — FEI 3002806434

The FDA completed an inspection of MEDTRONIC IRELAND on March 22, 2013 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
March 22, 2013
Fiscal Year
2013
Product Type
Devices
Project Area
Bioresearch Monitoring
Location
Galway (Ireland)

Additional Details

Postmarket Audit Inspections