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

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 · a18a27a5-384a-4ba4-9c27-1dd383cc8a67

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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