FDA Inspection
McRoberts, William Porter, MDMcRoberts, William Porter, MD – FDA Inspection, Nov 17, 2010
Record Details
This FDA Inspection record concerns McRoberts, William Porter, MD, with an inspection on November 17, 2010, issued by the Center for Devices and Radiological Health, covering devices.
- Inspection Date
- November 17, 2010
- Product Type
- Devices
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ID · 65d22967-6df2-426d-a385-384216d4e71e
Inspection Facts
Voluntary Action Indicated (VAI)
Objectionable conditions were found, but FDA is not prepared to take or recommend regulatory action.
- Inspection number
- 697560
- FDA center
- Medical Devices & Rad Health
- Project area
- Bioresearch Monitoring
FDA Citations
3- 21 CFR 812.150(a)(1)Investigator report of unanticipated adverse effects
- 21 CFR 812.100Investigator non-compliance with agreement/plan/regulations
- 21 CFR 812.100Investigator lack of informed consent
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