# FDA Inspection 1062606 - Genoray America Inc. - August 17, 2018

Source: https://www.keypedia.com/records/fda_inspections/genoray-america-inc/0ffbde47-cf5f-4137-a477-ecbd1752ce61
Source feed: FDA_Inspections

> FDA Inspection 1062606 for Genoray America Inc. on August 17, 2018. Classification: Voluntary Action Indicated (VAI).

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## Details

- Record Type: FDA Inspection
- Inspection ID: 1062606
- Company Name: Genoray America Inc.
- Inspection Date: 2018-08-17
- Classification: Voluntary Action Indicated (VAI)
- Project Area: Postmarket Assurance: Devices
- Product Type: Devices
- Office Name: Center for Devices and Radiological Health

## Related Documents

- [FDA Inspection 1062606 - 2018-08-17](https://www.keypedia.com/records/fda_inspections/genoray-america-inc/06fa9fb9-2354-4c90-b293-92f192114dea)

Company: https://www.keypedia.com/companies/genoray-america-inc/2883e76a-b9a9-4b90-9117-6a343785a936

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