FDA Inspection
St. Jude Medical, Atrial Fibrillation Division, Inc.St. Jude Medical, Atrial Fibrillation Division, Inc. – FDA Inspection, Jul 27, 2017
Record Details
This FDA Inspection record concerns St. Jude Medical, Atrial Fibrillation Division, Inc., with an inspection on July 27, 2017, issued by the Minneapolis District Office, covering medical devices & rad health.
- Inspection Date
- July 27, 2017
- Product Type
- Medical Devices & Rad Health
View Company Profile
ID · c5a99e2c-d5ae-4c1f-a7a9-e9da35e134fe
Inspection Facts
- Inspection number
- 1034622
- FDA center
- Medical Devices & Rad Health
- Outcome
- Form 483 issued
Other FDA inspections of St. Jude Medical, Atrial Fibrillation Division, Inc.
3| Date | Classification | Office | Project area |
|---|---|---|---|
| March 29, 2019 | NAI | Center for Devices and Radiological Health | Postmarket Assurance: Devices |
| May 17, 2018 | NAI | Center for Devices and Radiological Health | Bioresearch Monitoring |
| September 28, 2017 | NAI | Center for Devices and Radiological Health | Compliance: Devices |
Other documents for St. Jude Medical, Atrial Fibrillation Division, Inc.
- FDA Inspection 1084607 - 2019-03-29
- FDA Inspection 1053126 - 2018-05-17
- FDA Inspection 1029059 - 2017-09-28
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