FDA Inspection 601510 - Smith & Nephew, Inc. Advanced Surgical Devices Division - July 31, 2009

FDA Inspection 601510 for Smith & Nephew, Inc. Advanced Surgical Devices Division on July 31, 2009. Classification: Voluntary Action Indicated (VAI).

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Record Summary

FDA Inspection 601510 for Smith & Nephew, Inc. Advanced Surgical Devices Division on July 31, 2009. Classification: Voluntary Action Indicated (VAI).

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Record Information

Company

Smith & Nephew, Inc. Advanced Surgical Devices Division

Inspection Date

July 31, 2009

Product Type

Devices

Office

Center for Devices and Radiological Health

ID: fd28df17-7015-46d4-a61f-1bd86508dba6

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