FDA Inspection 762059 — Medtronic Inc

Medtronic Inc — FEI 3008770275

The FDA completed an inspection of Medtronic Inc on Jan 5, 2012 in Schiller Park, IL. 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
Jan 5, 2012
Fiscal Year
2012
Product Type
Devices
Project Area
Compliance: Devices
Location
Schiller Park, IL (United States)