FDA Inspection
Medtronic Xomed, Inc.Medtronic Xomed, Inc. – FDA Inspection, Jul 27, 2017
Record Details
This FDA Inspection record concerns Medtronic Xomed, Inc., with an inspection on July 27, 2017, issued by the Florida District Office, covering medical devices & rad health.
- Company
- Medtronic Xomed, Inc.
- Inspection Date
- July 27, 2017
- Product Type
- Medical Devices & Rad Health
- Office
- Florida District Office
View Company Profile
ID · 748e0b60-40dc-4039-9ebf-6c69bdb7d324
Inspection Facts
- Inspection number
- 1041671
- FDA center
- Medical Devices & Rad Health
- Outcome
- Form 483 issued
Other FDA inspections of Medtronic Xomed, Inc.
4| Date | Classification | Office | Project area |
|---|---|---|---|
| June 17, 2024 | VAI | Center for Devices and Radiological Health | Compliance: Devices |
| October 29, 2021 | VAI | Center for Devices and Radiological Health | Compliance: Devices |
| June 6, 2012 | NAI | Center for Devices and Radiological Health | Postmarket Assurance: Devices |
| December 19, 2008 | NAI | Center for Devices and Radiological Health | Compliance: Devices |
Other documents for Medtronic Xomed, Inc.
- FDA Inspection 1240536 - 2024-06-17
- FDA Inspection 1156931 - 2021-10-29
- FDA Inspection 786597 - 2012-06-06
- FDA Inspection 554176 - 2008-12-19
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