FDA WARNING_LETTER - Smith & Nephew Orthopaedics Gmbh - July 22, 2010

FDA WARNING_LETTER for Smith & Nephew Orthopaedics Gmbh on July 22, 2010. Product: Devices. Access full analysis and detailed observations.

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Record Summary

FDA WARNING_LETTER for Smith & Nephew Orthopaedics Gmbh on July 22, 2010. Product: Devices. Access full analysis and detailed observations.

Violation Codes

21 CFR 820.70(b)

21 CFR 820.90(b)

21 CFR 820

21 U.S.C. 321(h)

21 CFR 820.100(a)(4)

21 CFR 820.90(a)

21 U.S.C. 381(a)

21 CFR 820.75(a)

21 U.S.C. 351(h)

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Record Information

Company

Smith & Nephew Orthopaedics Gmbh

Inspection Date

July 22, 2010

Product Type

Devices

Office

Department of Health and Human Services

People

ID: 30ab902e-1e60-40ee-9ff5-73b7b52834de

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