FDA WARNING_LETTER - Anulex Technologies, Inc. - September 22, 2010

FDA WARNING_LETTER for Anulex Technologies, Inc. on September 22, 2010. Product: Devices. Access full analysis and detailed observations.

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Record Summary

FDA WARNING_LETTER for Anulex Technologies, Inc. on September 22, 2010. Product: Devices. Access full analysis and detailed observations.

Violation Codes

21 CFR 812.40

21 CFR 812

21 U.S.C. 360j(g)

21 CFR 812.3(m)

21 U.S.C. 351(f)(1)(B)

21 CFR 812.7(a)

21 CFR 812.20(a)(1)

21 U.S.C. 360(k)

21 CFR 812.7(d)

21 CFR 812.43(c)

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Record Information

Company

Anulex Technologies, Inc.

Inspection Date

September 22, 2010

Product Type

Devices

Office

Center for Devices and Radiological Health

People

ID: 694d7354-43a5-421b-8f61-b99dbc8c0b86

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