FDA Inspection 904708 — MEDTRONIC IRELAND

MEDTRONIC IRELAND — FEI 3002806434

The FDA completed an inspection of MEDTRONIC IRELAND on Nov 20, 2014 in Galway. The inspection was classified VAI (Voluntary Action Indicated — objectionable conditions or practices were found, but the agency is not prepared to take or recommend any administrative or regulatory action). Product area: Devices.

Inspection details

Classification
Voluntary Action Indicated (VAI)
End Date
Nov 20, 2014
Fiscal Year
2015
Product Type
Devices
Project Area
Project Evaluation: Devices
Location
Galway (Ireland)

Additional details

Postmarket Audit Inspections

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