# Koroad America, Inc. – FDA Inspection, May 1, 2019

Source: https://www.keypedia.com/records/fda_inspections/koroad-america-inc/b698cd4a-c4b5-4cab-b45f-401dec60557d
Source feed: FDA_Inspections

> FDA inspection 1088104 of Koroad America, Inc., May 01, 2019. Classification: Voluntary Action Indicated (VAI). 1 citation under 21 CFR part 820. Form 483 issued.

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## Details

- Record Type: FDA Inspection
- Inspection ID: 1088104
- Company Name: Koroad America, Inc.
- Inspection Date: 2019-05-01
- 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: 1

## Related Officers

- [Issuing Officer](https://www.keypedia.com/people/creighton-t-tuzon/be0d09c0-59f4-48c3-9e3d-a1ceb2587e3e)
- [Investigator](https://www.keypedia.com/people/eric-c-fox/218af117-1551-476f-80ba-172e2cd6baee)
- Issuing Officer
- [Investigator](https://www.keypedia.com/people/kevin-n-tran/dd74120c-4a8d-4fd0-9068-c862890d00d6)

Company: https://www.keypedia.com/companies/koroad-america-inc/fdb9cac6-4906-4cd2-b681-a7a5c5e92f5f

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