FDA Inspection 969542 - Randox Laboratories, Limited - April 28, 2016

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Record Details

This FDA Inspection record concerns Randox Laboratories, Limited, with an inspection on April 28, 2016, issued by the Center for Devices and Radiological Health, covering devices.

Company: Randox Laboratories, Limited
Inspection Date: April 28, 2016
Product Type: Devices
Office: Center for Devices and Radiological Health

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ID · 4fe2b409-5e0a-4615-8336-6b5e2f56d44e

Violation Codes1

21 CFR 820.198(a)

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