FDA Inspection 639866 - Isolux, LLC - January 22, 2010

FDA Inspection 639866 for Isolux, LLC on January 22, 2010. Classification: Voluntary Action Indicated (VAI).

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Record Summary

FDA Inspection 639866 for Isolux, LLC on January 22, 2010. Classification: Voluntary Action Indicated (VAI).

Violation Codes

21 CFR 803.17

21 CFR 820.198(a)

21 CFR 820.20(c)

21 CFR 820.30(a)

21 CFR 820.40

21 CFR 820.50

21 CFR 820.80(e)(3)

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Record Information

Company

Isolux, LLC

Inspection Date

January 22, 2010

Product Type

Devices

Office

Center for Devices and Radiological Health

ID: fda501d2-f18f-475f-a659-0e1496c16c80

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