# FDA Inspection 980091 - Onyx Healthcare - June 16, 2016

Source: https://www.keypedia.com/records/fda_inspections/onyx-healthcare/3ffef1bb-95e8-4a64-b5b5-58ed9394c95f
Source feed: FDA_Inspections

> FDA Inspection 980091 for Onyx Healthcare on June 16, 2016. Classification: No Action Indicated (NAI).

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## Details

- Record Type: FDA Inspection
- Inspection ID: 980091
- Company Name: Onyx Healthcare
- Inspection Date: 2016-06-16
- Classification: No Action Indicated (NAI)
- Project Area: Postmarket Assurance: Devices
- Product Type: Devices
- Office Name: Center for Devices and Radiological Health

## Related Documents

- [FDA Inspection 980091 - 2016-06-16](https://www.keypedia.com/records/fda_inspections/onyx-healthcare/7311f4cf-0ecc-4532-b1be-87df6ca2bf1c)

Company: https://www.keypedia.com/companies/onyx-healthcare/6cc2c500-cad9-47ea-acc5-1ecb4d3c836a

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