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 · 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

Full citation text and observation details available on the Dashboard.

FDA Inspection

NIPRO CANADA CORPORATIONOctober 20, 2016

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

Open in Dashboard

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

Full citation text and observation details available on the Dashboard.