# FDA Inspection 551172 - Stryker GmbH - November 06, 2008

Source: https://www.globalkeysolutions.net/records/fda_inspections/stryker-gmbh/e567f042-0d55-407a-91bb-1916e0478ada
Source feed: FDA_Inspections

> FDA Inspection 551172 for Stryker GmbH on November 06, 2008. Classification: Voluntary Action Indicated (VAI).

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## Details

- Record Type: FDA Inspection
- Inspection ID: 551172
- Company Name: Stryker GmbH
- Inspection Date: 2008-11-06
- Classification: Voluntary Action Indicated (VAI)
- 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-gmbh/c74b50c4-3566-425d-9331-7fb21b736586

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