FDA Inspection 606855 - Smith & Nephew Inc. - August 06, 2009

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Record Details

This FDA Inspection record concerns Smith & Nephew Inc., with an inspection on August 6, 2009, issued by the Center for Devices and Radiological Health, covering devices.

Company: Smith & Nephew Inc.
Inspection Date: August 6, 2009
Product Type: Devices
Office: Center for Devices and Radiological Health

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ID · 685a52fd-4d6a-4d7b-afb7-58a1979d77e5

Violation Codes2

21 CFR 820.30(g)21 CFR 820.75(c)

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