FDA Inspection 799542 - Affymetrix - September 26, 2012

FDA Inspection 799542 for Affymetrix on September 26, 2012. Classification: Voluntary Action Indicated (VAI).

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Record Summary

FDA Inspection 799542 for Affymetrix on September 26, 2012. Classification: Voluntary Action Indicated (VAI).

Violation Codes

21 CFR 806.20(a)

21 CFR 820.100(b)

21 CFR 820.50

21 CFR 820.72(a)

21 CFR 820.75(b)

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Record Information

Company

Affymetrix

Inspection Date

September 26, 2012

Product Type

Devices

Office

Center for Devices and Radiological Health

ID: f796dbcb-8d4c-40de-a9b0-86c7b60694ad

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