FDA Inspection 995281 - NIPRO CANADA CORPORATION - October 20, 2016

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Record Details

This FDA Inspection record concerns NIPRO CANADA CORPORATION, with an inspection on October 20, 2016, issued by the Center for Devices and Radiological Health, covering devices.

Company: NIPRO CANADA CORPORATION
Inspection Date: October 20, 2016
Product Type: Devices
Office: Center for Devices and Radiological Health

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ID · d94f6a3e-5e4a-40f6-8f8f-bd9d88862999

Violation Codes4

21 CFR 820.100(b)21 CFR 820.198(d)21 CFR 820.198(e)21 CFR 820.22

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