FDA WARNING_LETTER - DMX-Works, Inc. - July 01, 2012

FDA WARNING_LETTER for DMX-Works, Inc. on July 01, 2012. Product: Devices. Access full analysis and detailed observations.

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Record Summary

FDA WARNING_LETTER for DMX-Works, Inc. on July 01, 2012. Product: Devices. Access full analysis and detailed observations.

Violation Codes

21 CFR 820.70(b)

21 CFR 820.22

21 U.S.C. 360oo

21 CFR 820.50(a)

21 CFR 820.80(c)

21 CFR 820

21 CFR 820.200(b)

21 U.S.C. 321(h)

21 CFR 1002.13

21 CFR 1002.11

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Record Information

Company

DMX-Works, Inc.

Inspection Date

July 1, 2012

Product Type

Devices

Office

Florida District Office

People

ID: c16ee033-9987-420b-99c3-dba508e97f58

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