FDA Inspection 818020 - Viper Technologies, LLC dba Avalign Thortex - January 25, 2013

FDA Inspection 818020 for Viper Technologies, LLC dba Avalign Thortex on January 25, 2013. Classification: Voluntary Action Indicated (VAI).

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Record Summary

FDA Inspection 818020 for Viper Technologies, LLC dba Avalign Thortex on January 25, 2013. Classification: Voluntary Action Indicated (VAI).

Violation Codes

21 CFR 820.100(a)

21 CFR 820.198(a)

21 CFR 820.70(i)

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Record Information

Company

Viper Technologies, LLC dba Avalign Thortex

Inspection Date

January 25, 2013

Product Type

Devices

Office

Center for Devices and Radiological Health

ID: faa1005d-5760-41bd-b33b-127eb8ab5563

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