FDA Inspection 1020184 - Smith & Nephew, Inc. - August 02, 2017

FDA Inspection 1020184 for Smith & Nephew, Inc. on August 02, 2017. Classification: Voluntary Action Indicated (VAI).

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Record Summary

FDA Inspection 1020184 for Smith & Nephew, Inc. on August 02, 2017. Classification: Voluntary Action Indicated (VAI).

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Record Information

Company

Smith & Nephew, Inc.

Inspection Date

August 2, 2017

Product Type

Devices

Office

Center for Devices and Radiological Health

ID: fd39576a-b8ba-4bf3-b687-8febeb19e56d

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