FDA Inspection 975150 - InterX Technologies - June 03, 2016

FDA Inspection 975150 for InterX Technologies on June 03, 2016. Classification: Voluntary Action Indicated (VAI).

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Record Summary

FDA Inspection 975150 for InterX Technologies on June 03, 2016. Classification: Voluntary Action Indicated (VAI).

Violation Codes

21 CFR 820.100(a)

21 CFR 820.30(e)

21 CFR 820.30(f)

21 CFR 820.30(g)

21 CFR 820.30(i)

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Record Information

Company

InterX Technologies

Inspection Date

June 3, 2016

Product Type

Devices

Office

Center for Devices and Radiological Health

ID: f8d5fb64-7a65-4638-8668-da90a5d59677

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