FDA Inspection 1022962 - Van Duzen, Inc. dba MedCAD - August 23, 2017

Record Details

This FDA Inspection record concerns Van Duzen, Inc. dba MedCAD, with an inspection on August 23, 2017, issued by the Center for Devices and Radiological Health, covering devices.

Company: Van Duzen, Inc. dba MedCAD
Inspection Date: August 23, 2017
Product Type: Devices
Office: Center for Devices and Radiological Health

Open in Dashboard

ID · 10efa1ad-6709-4041-a364-c86f1c91e653

Violation Codes8

21 CFR 803.1721 CFR 820.100(a)21 CFR 820.198(a)21 CFR 820.2221 CFR 820.25(b)21 CFR 820.72(a)21 CFR 820.75(a)21 CFR 820.90(a)

Full citation text and observation details available on the Dashboard.