FDA WARNING_LETTER - Aionex Inc - November 20, 2012

FDA WARNING_LETTER for Aionex Inc on November 20, 2012. Product: Devices. Access full analysis and detailed observations.

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Record Summary

FDA WARNING_LETTER for Aionex Inc on November 20, 2012. Product: Devices. Access full analysis and detailed observations.

Violation Codes

21 CFR 820.22

21 U.S.C. 360(j)

21 CFR 820.25(b)

21 U.S.C. 360

21 CFR 820.100(a)

21 CFR 820

21 U.S.C. 321(h)

21 CFR 820.198(a)

21 CFR 820.20(c)

21 CFR 803

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Record Information

Company

Aionex Inc

Inspection Date

November 20, 2012

Product Type

Devices

Office

New Orleans District Office

People

ID: 7d299e41-17f3-4b26-9c89-353772c38459

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