# FDA Inspection 750642 - Stryker Spine - September 29, 2011

Source: https://www.keypedia.com/records/fda_inspections/stryker-spine/b785a1bb-07a6-46c4-aa21-7b5604f5b4cf
Source feed: FDA_Inspections

> FDA Inspection 750642 for Stryker Spine on September 29, 2011. Classification: Voluntary Action Indicated (VAI).

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## Details

- Record Type: FDA Inspection
- Inspection ID: 750642
- Company Name: Stryker Spine
- Inspection Date: 2011-09-29
- Classification: Voluntary Action Indicated (VAI)
- Project Area: Postmarket Assurance: Devices
- Product Type: Devices
- Office Name: Center for Devices and Radiological Health

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Company: https://www.keypedia.com/companies/stryker-spine/6cfbb80a-1ad5-4c55-90f8-8487e747b60c

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