# FDA Inspection 1088104 - Koroad America, Inc. - May 01, 2019

Source: https://www.keypedia.com/records/fda_inspections/koroad-america-inc/0aba1e40-2c9b-4f57-a8aa-be5ff8f63f62
Source feed: FDA_Inspections

> FDA Inspection 1088104 for Koroad America, Inc. on May 01, 2019. Classification: Voluntary Action Indicated (VAI).

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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)
- Project Area: Compliance: Devices
- Product Type: Devices
- Office Name: Center for Devices and Radiological Health

## Related Documents

- [FDA Inspection 1088104 - 2019-05-01](https://www.keypedia.com/records/fda_inspections/koroad-america-inc/b698cd4a-c4b5-4cab-b45f-401dec60557d)

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