FDA Inspection 861149 - RANDOX TEORANTA - December 05, 2013

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Record Details

This FDA Inspection record concerns RANDOX TEORANTA, with an inspection on December 5, 2013, issued by the Center for Devices and Radiological Health, covering devices.

Company: RANDOX TEORANTA
Inspection Date: December 5, 2013
Product Type: Devices
Office: Center for Devices and Radiological Health

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ID · 1cdafc37-bc29-453e-ae34-e0698b5dccfd

Violation Codes2

21 CFR 820.100(a)21 CFR 820.198(a)

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