# Van Duzen, Inc. dba MedCAD – FDA Inspection, Jan 30, 2019

Source: https://www.keypedia.com/records/fda_inspections/van-duzen-inc-dba-medcad/c00d99be-c0d5-439d-a3ea-f85d0a8c1018
Source feed: FDA_Inspections

> FDA inspection 1077558 of Van Duzen, Inc. dba MedCAD, January 30, 2019. Classification: Voluntary Action Indicated (VAI). 4 citations under 21 CFR parts 803 and 820. Form 483 issued. 3 other FDA inspections on record for this company.

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## Details

- Record Type: FDA Inspection
- Inspection ID: 1077558
- Company Name: Van Duzen, Inc. dba MedCAD
- Inspection Date: 2019-01-30
- Classification: Voluntary Action Indicated (VAI)
- Classification Code: VAI
- Project Area: Postmarket Assurance: Devices
- Product Type: Devices
- Center: Medical Devices & Rad Health
- Office Name: Center for Devices and Radiological Health
- Citation Count: 4

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## Related Officers

- [Company Rep](https://www.keypedia.com/people/roy-baby/69a18ef5-167c-41eb-a57e-3d138a0820c2)

Company: https://www.keypedia.com/companies/van-duzen-inc-dba-medcad/23639a02-cad0-4bd2-a9e7-016970fd114d

Office: https://www.keypedia.com/offices/center-for-devices-and-radiological-health/9d89aff6-e435-4764-87be-f58c01aca7f7