FDA Inspection
Stryker Neurovascular, Inc.Stryker Neurovascular, Inc. – FDA Inspection, Feb 2, 2009
Record Details
This FDA Inspection record concerns Stryker Neurovascular, Inc., with an inspection on February 2, 2009, issued by the Center for Devices and Radiological Health, covering devices.
- Company
- Stryker Neurovascular, Inc.
- Inspection Date
- February 2, 2009
- Product Type
- Devices
View Company Profile
ID · 09478f31-0029-4065-9abb-b2bdfa8d4f31
Inspection Facts
No Action Indicated (NAI)
No objectionable conditions or practices were found during the inspection.
- Inspection number
- 561509
- FDA center
- Medical Devices & Rad Health
- Project area
- Compliance: Devices
Other FDA inspections of Stryker Neurovascular, Inc.
4| Date | Classification | Office | Project area |
|---|---|---|---|
| May 3, 2024 | NAI | Center for Devices and Radiological Health | Compliance: Devices |
| January 18, 2018 | Not classified | Denver District Office | |
| December 2, 2015 | NAI | Center for Devices and Radiological Health | Postmarket Assurance: Devices |
| November 1, 2012 | NAI | Center for Devices and Radiological Health | Postmarket Assurance: Devices |
Other documents for Stryker Neurovascular, Inc.
- FDA Inspection 1229210 - 2024-05-03
- FDA Inspection 1039088 - 2018-01-18
- FDA Inspection 956410 - 2015-12-02
- FDA Inspection 805526 - 2012-11-01
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