# FDA Inspection 595638 - Stryker Osteosynthesis Freiburg - May 29, 2009

Source: https://www.keypedia.com/records/fda_inspections/stryker-osteosynthesis-freiburg/c4b2c086-adf4-4252-908f-dbfdcab5f913
Source feed: FDA_Inspections

> FDA Inspection 595638 for Stryker Osteosynthesis Freiburg on May 29, 2009. Classification: No Action Indicated (NAI).

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## Details

- Record Type: FDA Inspection
- Inspection ID: 595638
- Company Name: Stryker Osteosynthesis Freiburg
- Inspection Date: 2009-05-29
- Classification: No Action Indicated (NAI)
- Project Area: Compliance: Devices
- Product Type: Devices
- Office Name: Center for Devices and Radiological Health

Company: https://www.keypedia.com/companies/stryker-osteosynthesis-freiburg/b0b8370c-e645-480e-902f-d1925e7baa5e

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