FDA Inspection 620825 - Smith & Nephew Orthopaedics AG - September 10, 2009

FDA Inspection 620825 for Smith & Nephew Orthopaedics AG on September 10, 2009. Classification: No Action Indicated (NAI).

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Record Summary

FDA Inspection 620825 for Smith & Nephew Orthopaedics AG on September 10, 2009. Classification: No Action Indicated (NAI).

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Record Information

Company

Smith & Nephew Orthopaedics AG

Inspection Date

September 10, 2009

Product Type

Devices

Office

Center for Devices and Radiological Health

ID: fa637e42-8cc1-482b-8f3f-3ef60ad3d540

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