FDA Inspection 935470 - Smith & Nephew Inc - July 23, 2015

FDA Inspection 935470 for Smith & Nephew Inc on July 23, 2015. Classification: No Action Indicated (NAI).

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Record Summary

FDA Inspection 935470 for Smith & Nephew Inc on July 23, 2015. Classification: No Action Indicated (NAI).

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Record Information

Company

Smith & Nephew Inc

Inspection Date

July 23, 2015

Product Type

Devices

Office

Center for Devices and Radiological Health

ID: fc7769d2-a94e-4141-bdc6-19f3c733f0ac

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