FDA Inspection 1031401 — St. Jude Medical

St. Jude Medical — FEI 3012179728

The FDA completed an inspection of St. Jude Medical on October 30, 2017 in Roseville, 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
October 30, 2017
Fiscal Year
2018
Product Type
Devices
Project Area
Bioresearch Monitoring
Location
Roseville, MN (United States)

Additional Details

Postmarket Audit Inspections