# Van Duzen, Inc. dba MedCAD – FDA Inspection, Aug 23, 2017

Source: https://www.keypedia.com/records/fda_inspections/van-duzen-inc-dba-medcad/40119ee4-056e-43c5-a71e-32046a711e90
Source feed: FDA_Inspections

> FDA inspection 1022962 of Van Duzen, Inc. dba MedCAD, August 23, 2017. Classification: Official Action Indicated (OAI). 8 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: 1022962
- Company Name: Van Duzen, Inc. dba MedCAD
- Inspection Date: 2017-08-23
- Classification: Official Action Indicated (OAI)
- Classification Code: OAI
- Project Area: Postmarket Assurance: Devices
- Product Type: Devices
- Center: Medical Devices & Rad Health
- Office Name: Center for Devices and Radiological Health
- Citation Count: 8

## Related Documents

- [FDA Inspection 1245727 - 2024-08-02](https://www.keypedia.com/records/fda_inspections/van-duzen-inc-dba-medcad/a8861bcd-2b4f-4474-b488-565a1ce8e59c)
- [FDA Inspection 1077558 - 2019-01-30](https://www.keypedia.com/records/fda_inspections/van-duzen-inc-dba-medcad/c00d99be-c0d5-439d-a3ea-f85d0a8c1018)
- [FDA Inspection 818525 - 2013-02-15](https://www.keypedia.com/records/fda_inspections/van-duzen-inc-dba-medcad/92ee4442-00de-45e0-8dcb-d19b0662958e)

## Related Officers

- [Issuing Officer](https://www.keypedia.com/people/karen-m-cruz-arenas/6c698301-84ca-4ba7-a79c-309721db2f1b)

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