FDA Inspection 1026395 - HQ, Inc. - September 22, 2017

Record Details

This FDA Inspection record concerns HQ, Inc., with an inspection on September 22, 2017, issued by the Center for Devices and Radiological Health, covering devices.

Company: HQ, Inc.
Inspection Date: September 22, 2017
Product Type: Devices
Office: Center for Devices and Radiological Health

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ID · dfd24615-95ee-4403-8e77-5246b6cd6194

Violation Codes8

21 CFR 803.1721 CFR 820.100(a)21 CFR 820.198(c)21 CFR 820.40(a)21 CFR 820.5021 CFR 820.70(a)21 CFR 820.8621 CFR 820.90(a)

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