# FDA Inspection 998485 - Patrick Hurban - January 20, 2017

Source: https://www.keypedia.com/records/fda_inspections/patrick-hurban/481ba6c1-8542-4eea-b3ce-038ba6877a43
Source feed: FDA_Inspections

> FDA Inspection 998485 for Patrick Hurban on January 20, 2017. Classification: No Action Indicated (NAI).

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## Details

- Record Type: FDA Inspection
- Inspection ID: 998485
- Company Name: Patrick Hurban
- Inspection Date: 2017-01-20
- Classification: No Action Indicated (NAI)
- Project Area: Bioresearch Monitoring
- Product Type: Devices
- Office Name: Center for Devices and Radiological Health

## Related Documents

- [FDA Inspection 1114504 - 2019-12-12](https://www.keypedia.com/records/fda_inspections/patrick-hurban/38c2519b-19cd-40b9-896f-a5c2ed6bc53d)

Company: https://www.keypedia.com/companies/patrick-hurban/4aa8364e-a387-43af-a3e8-4de649fcf997

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