FDA Inspection 956232 - Oxus, Inc. - January 19, 2016

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Record Details

This FDA Inspection record concerns Oxus, Inc., with an inspection on January 19, 2016, issued by the Center for Devices and Radiological Health, covering devices.

Company: Oxus, Inc.
Inspection Date: January 19, 2016
Product Type: Devices
Office: Center for Devices and Radiological Health

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ID · 38ca1d3a-6f3b-4aec-8a53-ad83f0bfa489

Violation Codes5

21 CFR 806.20(b)(4)21 CFR 820.30(a)21 CFR 820.30(i)21 CFR 820.80(d)21 CFR 820.90(a)

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