# FDA Inspection 763943 - Stryker Spine - January 12, 2012

Source: https://www.globalkeysolutions.net/records/fda_inspections/stryker-spine/f89db674-3c63-4c7f-9dca-799d47ec9669/
Source feed: FDA_Inspections

> FDA Inspection 763943 for Stryker Spine on January 12, 2012. Classification: No Action Indicated (NAI).

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## Details

- Record Type: FDA Inspection
- Inspection ID: 763943
- Company Name: Stryker Spine
- Inspection Date: 2012-01-12
- Classification: No Action Indicated (NAI)
- Project Area: Compliance: Devices
- Product Type: Devices
- Office Name: Center for Devices and Radiological Health

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Company: https://www.globalkeysolutions.net/companies/stryker-spine/9eecc83b-d4a3-4769-830f-9d237adc74e5

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