FDA Inspection
Medtronic Heart Valves DivisionMedtronic Heart Valves Division – FDA Inspection, Mar 30, 2016
Record Details
This FDA Inspection record concerns Medtronic Heart Valves Division, with an inspection on March 30, 2016, issued by the Center for Devices and Radiological Health, covering devices.
- Inspection Date
- March 30, 2016
- Product Type
- Devices
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ID · d3877afe-2161-41e1-a843-bdb279a4d66b
Inspection Facts
No Action Indicated (NAI)
No objectionable conditions or practices were found during the inspection.
- Inspection number
- 965285
- FDA center
- Medical Devices & Rad Health
- Project area
- Postmarket Assurance: Devices
Other FDA inspections of Medtronic Heart Valves Division
6| Date | Classification | Office | Project area |
|---|---|---|---|
| October 26, 2020 | NAI | Center for Devices and Radiological Health | Compliance: Devices |
| March 9, 2015 | NAI | Center for Devices and Radiological Health | Bioresearch Monitoring |
| March 7, 2014 | NAI | Center for Devices and Radiological Health | Postmarket Assurance: Devices |
| September 3, 2013 | NAI | Center for Devices and Radiological Health | Compliance: Devices |
| June 24, 2010 | VAI | Center for Devices and Radiological Health | Compliance: Devices |
Other documents for Medtronic Heart Valves Division
- FDA Inspection 1131979 - 2020-10-26
- FDA Inspection 917203 - 2015-03-09
- FDA Inspection 870529 - 2014-03-07
- FDA Inspection 850644 - 2013-09-03
- FDA Inspection 669393 - 2010-06-24
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