FDA Inspection 1152056 - CardioQuip, LLC - September 17, 2021

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Record Details

This FDA Inspection record concerns CardioQuip, LLC, with an inspection on September 17, 2021, issued by the Center for Devices and Radiological Health, covering devices.

Company: CardioQuip, LLC
Inspection Date: September 17, 2021
Product Type: Devices
Office: Center for Devices and Radiological Health

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ID · fd25d0ae-a8f6-4e94-9319-165cb7d4bc78

Violation Codes10

21 CFR 803.1721 CFR 820.100(b)21 CFR 820.198(a)21 CFR 820.198(b)21 CFR 820.198(d)21 CFR 820.200(a)21 CFR 820.30(c)21 CFR 820.30(d)21 CFR 820.30(g)21 CFR 820.30(i)

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