FDA Inspection 1029059 — St. Jude Medical, Atrial Fibrillation Division, Inc.
The FDA completed an inspection of St. Jude Medical, Atrial Fibrillation Division, Inc. on September 28, 2017 in Saint Paul, 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
- September 28, 2017
- Fiscal Year
- 2017
- Product Type
- Devices
- Project Area
- Compliance: Devices
- Location
- Saint Paul, MN (United States)