FDA Inspection 975150 - InterX Technologies - June 03, 2016

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Record Details

This FDA Inspection record concerns InterX Technologies, with an inspection on June 3, 2016, issued by the Center for Devices and Radiological Health, covering devices.

Company: InterX Technologies
Inspection Date: June 3, 2016
Product Type: Devices
Office: Center for Devices and Radiological Health

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ID · c3315d95-7b51-4cae-ba31-935d34deb38f

Violation Codes5

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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