FDA Inspection 823591 — MEDTRONIC IRELAND

MEDTRONIC IRELAND — FEI 3002806434

The FDA completed an inspection of MEDTRONIC IRELAND on Mar 22, 2013 in Galway. The inspection was classified NAI (No Action Indicated — no objectionable conditions or practices were found during the inspection). Product area: Devices.

Inspection details

Classification
No Action Indicated (NAI)
End Date
Mar 22, 2013
Fiscal Year
2013
Product Type
Devices
Project Area
Project Evaluation: Devices
Location
Galway (Ireland)

Additional details

Postmarket Audit Inspections

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