FDA Inspection
Medtronic NeuromodulationMedtronic Neuromodulation – FDA Inspection, May 9, 2012
Record Details
This FDA Inspection record concerns Medtronic Neuromodulation, with an inspection on May 9, 2012, issued by the Center for Devices and Radiological Health, covering devices.
- Company
- Medtronic Neuromodulation
- Inspection Date
- May 9, 2012
- Product Type
- Devices
View Company Profile
ID · e0be1944-104a-4c50-a4ba-e6b8055c7aa9
Inspection Facts
Official Action Indicated (OAI)
Significant objectionable conditions were found and regulatory or administrative action is recommended.
- Inspection number
- 774200
- FDA center
- Medical Devices & Rad Health
- Project area
- Compliance: Devices
Other FDA inspections of Medtronic Neuromodulation
15| Date | Classification | Office | Project area |
|---|---|---|---|
| May 5, 2023 | VAI | Center for Devices and Radiological Health | Postmarket Assurance: Devices |
| November 3, 2022 | VAI | Center for Devices and Radiological Health | Postmarket Assurance: Devices |
| September 9, 2021 | NAI | Center for Devices and Radiological Health | Compliance: Devices |
| October 17, 2019 | VAI | Center for Devices and Radiological Health | Compliance: Devices |
| August 6, 2019 | NAI | Center for Devices and Radiological Health | Compliance: Devices |
Other documents for Medtronic Neuromodulation
- FDA Inspection 1206222 - 2023-05-05
- FDA Inspection 1187313 - 2022-11-03
- FDA Inspection 1153966 - 2021-09-09
- FDA Inspection 1108789 - 2019-10-17
- FDA Inspection 1102180 - 2019-08-06
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