# Codan US Corporation – FDA Inspection, Jul 20, 2018

Source: https://www.keypedia.com/records/fda_inspections/codan-us-corporation/ac5ea224-cd5e-4661-8972-80afc07d5213
Source feed: FDA_Inspections

> FDA inspection 1059719 of Codan US Corporation, July 20, 2018. Classification: Voluntary Action Indicated (VAI). 1 citation under 21 CFR part 820. Form 483 issued. 2 other FDA inspections on record for this company.

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## Details

- Record Type: FDA Inspection
- Inspection ID: 1059719
- Company Name: Codan US Corporation
- Inspection Date: 2018-07-20
- Classification: Voluntary Action Indicated (VAI)
- Classification Code: VAI
- Project Area: Compliance: Devices
- Product Type: Devices
- Center: Medical Devices & Rad Health
- Office Name: Center for Devices and Radiological Health
- Citation Count: 1

## Related Documents

- FDA Inspection 883590 - 2014-06-18
- FDA Inspection 612137 - 2009-09-16

## Related Officers

- [Company Rep](https://www.keypedia.com/people/paul-m-kawamoto/0a24b110-12de-4736-8d98-7a023ceec01e)

Company: https://www.keypedia.com/companies/codan-us-corporation/ddd42719-5c53-420d-a8b9-b5bd709373c3

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