FDA Inspection
Derek H. JonesDerek H. Jones – FDA Inspection, Oct 23, 2009
Record Details
This FDA Inspection record concerns Derek H. Jones, with an inspection on October 23, 2009, issued by the Center for Devices and Radiological Health, covering devices.
- Company
- Derek H. Jones
- Inspection Date
- October 23, 2009
- Product Type
- Devices
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ID · e3a51823-6336-4f54-9b79-56b7b5a90467
Inspection Facts
Voluntary Action Indicated (VAI)
Objectionable conditions were found, but FDA is not prepared to take or recommend regulatory action.
- Inspection number
- 626330
- FDA center
- Medical Devices & Rad Health
- Project area
- Bioresearch Monitoring
FDA Citations
1- 21 CFR 812.140(a)(3)(ii)Investigator records of relevant observations inadequate
Full citation text and observation details available on the Dashboard.
Other FDA inspections of Derek H. Jones
2| Date | Classification | Office | Project area |
|---|---|---|---|
| February 21, 2020 | NAI | Center for Devices and Radiological Health | Bioresearch Monitoring |
| October 19, 2017 | NAI | Center for Drug Evaluation and Research | Bioresearch Monitoring |
Other documents for Derek H. Jones
- FDA Inspection 1119256 - 2020-02-21
- FDA Inspection 1033820 - 2017-10-19
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