# FDA Inspection 555056 - Smith & Nephew Orthopaedics GmbH - November 13, 2008

Source: https://www.keypedia.com/records/fda_inspections/smith-nephew-orthopaedics-gmbh/e292d5d0-ce2f-4405-bdaa-e497d3ebefa2
Source feed: FDA_Inspections

> FDA Inspection 555056 for Smith & Nephew Orthopaedics GmbH on November 13, 2008. Classification: Voluntary Action Indicated (VAI).

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## Details

- Record Type: FDA Inspection
- Inspection ID: 555056
- Company Name: Smith & Nephew Orthopaedics GmbH
- Inspection Date: 2008-11-13
- 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/smith-nephew-orthopaedics-gmbh/65d3d2bd-0c5f-486d-ab89-d6c131368645

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