FDA Inspection 1031401 — St. Jude Medical

St. Jude Medical — FEI 3012179728

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

Additional Details

Postmarket Audit Inspections

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