# FDA Inspection 1119256 - Derek H. Jones - February 21, 2020

Source: https://www.keypedia.com/records/fda_inspections/derek-h-jones/d7c372e2-97de-4d32-b9e7-eed62f165c93
Source feed: FDA_Inspections

> FDA Inspection 1119256 for Derek H. Jones on February 21, 2020. Classification: No Action Indicated (NAI).

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## Details

- Record Type: FDA Inspection
- Inspection ID: 1119256
- Company Name: Derek H. Jones
- Inspection Date: 2020-02-21
- Classification: No Action Indicated (NAI)
- Project Area: Bioresearch Monitoring
- Product Type: Devices
- Office Name: Center for Devices and Radiological Health

## Related Documents

- [FDA Inspection 1033820 - 2017-10-19](https://www.keypedia.com/records/fda_inspections/derek-h-jones/1bcb30bc-1b5b-4652-990f-aadcbd1a7c69)
- [FDA Inspection 626330 - 2009-10-23](https://www.keypedia.com/records/fda_inspections/derek-h-jones/e3a51823-6336-4f54-9b79-56b7b5a90467)

Company: https://www.keypedia.com/companies/derek-h-jones/53f3936a-efb3-46d7-9930-3756ecafe3f6

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