# Stryker Neurovascular – FDA Inspection, Oct 16, 2017

Source: https://www.keypedia.com/records/fda_inspections/stryker-neurovascular/830feb26-c340-4730-a20c-71c55f4e6fc9
Source feed: FDA_Inspections

> FDA inspection 1028734 of Stryker Neurovascular, October 16, 2017. Classification: Voluntary Action Indicated (VAI). 3 citations under 21 CFR parts 803 and 820. Form 483 issued. 6 other FDA inspections on record for this company.

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## Details

- Record Type: FDA Inspection
- Inspection ID: 1028734
- Company Name: Stryker Neurovascular
- Inspection Date: 2017-10-16
- Classification: Voluntary Action Indicated (VAI)
- Classification Code: VAI
- Project Area: Compliance: Devices
- Product Type: Devices
- Center: Medical Devices & Rad Health
- Office Name: Center for Devices and Radiological Health
- Citation Count: 3

## Related Documents

- [FDA Inspection 1257117 - 2024-12-18](https://www.keypedia.com/records/fda_inspections/stryker-neurovascular/8d0493c2-985c-4955-86c1-f6f0f5fa478d)
- FDA Inspection 1032404 - 2017-09-22
- FDA Inspection 980716 - 2016-06-01
- FDA Inspection 936471 - 2015-07-30
- FDA Inspection 851608 - 2013-10-15

## Related Officers

- [FDA Associated Person](https://www.keypedia.com/people/james-a-lane/f6cd3d8d-7de9-45c5-9380-7e0c5de4720e)

Company: https://www.keypedia.com/companies/stryker-neurovascular/75d76f13-3dbc-4078-a970-3bf0cbbf5a7b

Office: https://www.keypedia.com/offices/center-for-devices-and-radiological-health/9d89aff6-e435-4764-87be-f58c01aca7f7