FDA Inspection 1053126 — St. Jude Medical, Atrial Fibrillation Division, Inc.
The FDA completed an inspection of St. Jude Medical, Atrial Fibrillation Division, Inc. on May 17, 2018 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
- May 17, 2018
- Fiscal Year
- 2018
- Product Type
- Devices
- Project Area
- Bioresearch Monitoring
- Location
- Saint Paul, MN (United States)
Additional Details
Postmarket Audit Inspections