# FDA Inspection 590920 - STRYKER IRELAND OSTEONICS - May 21, 2009

Source: https://www.keypedia.com/records/fda_inspections/stryker-ireland-osteonics/bceb0899-99cb-44f7-b7ee-4e28dbe8f337
Source feed: FDA_Inspections

> FDA Inspection 590920 for STRYKER IRELAND OSTEONICS on May 21, 2009. Classification: Voluntary Action Indicated (VAI).

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## Details

- Record Type: FDA Inspection
- Inspection ID: 590920
- Company Name: STRYKER IRELAND OSTEONICS
- Inspection Date: 2009-05-21
- 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.keypedia.com/companies/stryker-ireland-osteonics/870d4adc-f348-4b35-a99d-6f9af28f9a12

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