FDA Inspection
Thomas K Jones MD - Clinical InvestigatorThomas K Jones MD - Clinical Investigator – FDA Inspection, Mar 19, 2009
Record Details
This FDA Inspection record concerns Thomas K Jones MD - Clinical Investigator, with an inspection on March 19, 2009, issued by the Center for Devices and Radiological Health, covering devices.
- Inspection Date
- March 19, 2009
- Product Type
- Devices
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ID · 995b9d81-7d14-435d-b954-73ac39bfd05a
Inspection Facts
Official Action Indicated (OAI)
Significant objectionable conditions were found and regulatory or administrative action is recommended.
- Inspection number
- 574553
- FDA center
- Medical Devices & Rad Health
- Project area
- Bioresearch Monitoring
FDA Citations
5- 21 CFR 812.110(b)Investigator non-compliance with agreement/plan/regulations
- 21 CFR 50.27(a)Consent form not approved/signed/dated
- 21 CFR 812.140(a)(3)Investigator"s subject records inadequate
- 21 CFR 812.140(a)(2)(i)Investigator device accountability inadequate
- 21 CFR 812.140(a)(1)Investigator correspondence records 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 |
| January 18, 2011 | VAI | 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 706952 - 2011-01-18
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