FDA Inspection
Suzanne Bruce, M.D.Suzanne Bruce, M.D. – FDA Inspection, Aug 3, 2012
Record Details
This FDA Inspection record concerns Suzanne Bruce, M.D., with an inspection on August 3, 2012, issued by the Center for Devices and Radiological Health, covering devices.
- Company
- Suzanne Bruce, M.D.
- Inspection Date
- August 3, 2012
- Product Type
- Devices
View Company Profile
ID · 88290129-bd9a-4293-b3da-eadb769f4077
Inspection Facts
Voluntary Action Indicated (VAI)
Objectionable conditions were found, but FDA is not prepared to take or recommend regulatory action.
- Inspection number
- 794721
- FDA center
- Medical Devices & Rad Health
- Project area
- Bioresearch Monitoring
FDA Citations
3- 21 CFR 812.100Investigator non-compliance with agreement/plan/regulations
- 21 CFR 812.100Investigator lack of informed consent
- 21 CFR 812.140(a)(3)Investigator"s subject records inadequate
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Other FDA inspections of Suzanne Bruce, M.D.
4| Date | Classification | Office | Project area |
|---|---|---|---|
| June 11, 2020 | NAI | Center for Drug Evaluation and Research | Bioresearch Monitoring |
| August 23, 2011 | NAI | Center for Drug Evaluation and Research | Bioresearch Monitoring |
| July 17, 2009 | NAI | Center for Biologics Evaluation and Research | Bioresearch Monitoring |
| March 19, 2009 | NAI | Center for Devices and Radiological Health | Bioresearch Monitoring |
Other documents for Suzanne Bruce, M.D.
- FDA Inspection 1124193 - 2020-06-11
- FDA Inspection 744842 - 2011-08-23
- FDA Inspection 598996 - 2009-07-17
- FDA Inspection 571172 - 2009-03-19
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