FDA Inspection 967750 — St. Jude Medical

St. Jude Medical — FEI 2182269

The FDA completed an inspection of St. Jude Medical on April 11, 2016 in Minnetonka, MN. 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
April 11, 2016
Fiscal Year
2016
Product Type
Devices
Project Area
Compliance: Devices
Location
Minnetonka, MN (United States)