FDA Inspection 984221 - CardioQuip, LLC - August 09, 2016

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Record Details

This FDA Inspection record concerns CardioQuip, LLC, with an inspection on August 9, 2016, issued by the Center for Devices and Radiological Health, covering devices.

Company: CardioQuip, LLC
Inspection Date: August 9, 2016
Product Type: Devices
Office: Center for Devices and Radiological Health

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ID · 5f4c1ebb-4e2f-4134-8f11-f9977da5b454

Violation Codes6

21 CFR 803.1721 CFR 820.100(a)21 CFR 820.198(a)21 CFR 820.30(i)21 CFR 820.50(a)(3)21 CFR 820.75(b)

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