# Derek H. Jones – FDA Inspection, Oct 23, 2009

Source: https://www.keypedia.com/records/fda_inspections/derek-h-jones/e3a51823-6336-4f54-9b79-56b7b5a90467
Source feed: FDA_Inspections

> FDA inspection 626330 of Derek H. Jones, October 23, 2009. Classification: Voluntary Action Indicated (VAI). 1 citation under 21 CFR part 812. 2 other FDA inspections on record for this company.

---

## Details

- Record Type: FDA Inspection
- Inspection ID: 626330
- Company Name: Derek H. Jones
- Inspection Date: 2009-10-23
- Classification: Voluntary Action Indicated (VAI)
- Classification Code: VAI
- Project Area: Bioresearch Monitoring
- Product Type: Devices
- Center: Medical Devices & Rad Health
- Office Name: Center for Devices and Radiological Health
- Citation Count: 1

## Related Documents

- [FDA Inspection 1119256 - 2020-02-21](https://www.keypedia.com/records/fda_inspections/derek-h-jones/d7c372e2-97de-4d32-b9e7-eed62f165c93)
- FDA Inspection 1033820 - 2017-10-19

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