FDA Inspection
Sue Ellen Cox, M.D.Sue Ellen Cox, M.D. – FDA Inspection, Jun 25, 2010
Record Details
This FDA Inspection record concerns Sue Ellen Cox, M.D., with an inspection on June 25, 2010, issued by the Center for Devices and Radiological Health, covering devices.
- Company
- Sue Ellen Cox, M.D.
- Inspection Date
- June 25, 2010
- Product Type
- Devices
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ID · 1ee415b6-c2d6-469f-b781-b4c468e170ac
Inspection Facts
Voluntary Action Indicated (VAI)
Objectionable conditions were found, but FDA is not prepared to take or recommend regulatory action.
- Inspection number
- 673484
- FDA center
- Medical Devices & Rad Health
- Project area
- Bioresearch Monitoring
FDA Citations
4- 21 CFR 812.100Investigator non-compliance with agreement/plan/regulations
- 21 CFR 812.100Investigator lack of informed consent
- 21 CFR 312.62(a)Accountability records
- 21 CFR 312.66Changes in research
Full citation text and observation details available on the Dashboard.
Other FDA inspections of Sue Ellen Cox, M.D.
3| Date | Classification | Office | Project area |
|---|---|---|---|
| May 16, 2025 | NAI | Center for Devices and Radiological Health | Bioresearch Monitoring |
| October 7, 2021 | NAI | Center for Drug Evaluation and Research | Bioresearch Monitoring |
| April 28, 2017 | NAI | Center for Devices and Radiological Health | Bioresearch Monitoring |
Other documents for Sue Ellen Cox, M.D.
- FDA Inspection 1270919 - 2025-05-16
- FDA Inspection 1155172 - 2021-10-07
- FDA Inspection 1010197 - 2017-04-28
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