FDA Inspection
Medtronic Sofamor Danek USA IncMedtronic Sofamor Danek USA Inc – FDA Inspection, May 3, 2017
Record Details
This FDA Inspection record concerns Medtronic Sofamor Danek USA Inc, with an inspection on May 3, 2017, issued by the New Orleans District Office, covering medical devices & rad health.
- Inspection Date
- May 3, 2017
- Product Type
- Medical Devices & Rad Health
View Company Profile
ID · 8a05b2e9-77b6-48d5-a949-5271c40a26ac
Inspection Facts
- Inspection number
- 1029473
- FDA center
- Medical Devices & Rad Health
- Outcome
- Form 483 issued
Other FDA inspections of Medtronic Sofamor Danek USA Inc
12| Date | Classification | Office | Project area |
|---|---|---|---|
| February 6, 2026 | NAI | Bioresearch Monitoring | |
| November 3, 2015 | VAI | Center for Devices and Radiological Health | Bioresearch Monitoring |
| October 23, 2015 | NAI | Center for Devices and Radiological Health | Postmarket Assurance: Devices |
| March 11, 2014 | VAI | Center for Devices and Radiological Health | Compliance: Devices |
| July 15, 2013 | NAI | Center for Devices and Radiological Health | Bioresearch Monitoring |
Other documents for Medtronic Sofamor Danek USA Inc
- FDA Inspection 1302636 - 2026-02-06
- FDA Inspection 950920 - 2015-11-03
- FDA Inspection 946127 - 2015-10-23
- FDA Inspection 869386 - 2014-03-11
- FDA Inspection 845563 - 2013-07-15
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