FDA Inspection
Thomas K Jones MD - Clinical InvestigatorThomas K Jones MD - Clinical Investigator – FDA Inspection, Jan 18, 2011
Record Details
This FDA Inspection record concerns Thomas K Jones MD - Clinical Investigator, with an inspection on January 18, 2011, issued by the Center for Devices and Radiological Health, covering devices.
- Inspection Date
- January 18, 2011
- Product Type
- Devices
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ID · 0b79b175-9ddf-4efe-a615-eef330c718bb
Inspection Facts
Voluntary Action Indicated (VAI)
Objectionable conditions were found, but FDA is not prepared to take or recommend regulatory action.
- Inspection number
- 706952
- 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 812.150(a)(7)Investigator report in response to a request
- 21 CFR 812.150(a)(4)No approval for investigator change in non-emergency
- 21 CFR 812.140(a)(2)(i)Investigator device accountability inadequate
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Other FDA inspections of Thomas K Jones MD - Clinical Investigator
2| Date | Classification | Office | Project area |
|---|---|---|---|
| December 16, 2015 | NAI | Center for Devices and Radiological Health | Bioresearch Monitoring |
| March 19, 2009 | OAI | Center for Devices and Radiological Health | Bioresearch Monitoring |
Other documents for Thomas K Jones MD - Clinical Investigator
- FDA Inspection 955628 - 2015-12-16
- FDA Inspection 574553 - 2009-03-19
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