FDA Inspection
Dianne Georgian-Smith,, M.D.Dianne Georgian-Smith,, M.D. – FDA Inspection, Oct 1, 2014
Record Details
This FDA Inspection record concerns Dianne Georgian-Smith,, M.D., with an inspection on October 1, 2014, issued by the Center for Devices and Radiological Health, covering devices.
- Company
- Dianne Georgian-Smith,, M.D.
- Inspection Date
- October 1, 2014
- Product Type
- Devices
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ID · 0ab42b89-170c-4032-a190-72aaa306d0bf
Inspection Facts
Voluntary Action Indicated (VAI)
Objectionable conditions were found, but FDA is not prepared to take or recommend regulatory action.
- Inspection number
- 901262
- FDA center
- Medical Devices & Rad Health
- Project area
- Bioresearch Monitoring
FDA Citations
2- 21 CFR 812.140(a)(3)(i)Investigator records of informed consent inadequate
- 21 CFR 812.140(d)Record retention inadequate
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