FDA Inspection 697560 — McRoberts, William Porter, MD

McRoberts, William Porter, MD — FEI 3008627160

The FDA completed an inspection of McRoberts, William Porter, MD on Nov 17, 2010 in Ft Lauderdale, FL. The inspection was classified VAI (Voluntary Action Indicated — objectionable conditions or practices were found, but the agency is not prepared to take or recommend any administrative or regulatory action). 3 citations were issued during this inspection. Product area: Devices.

Inspection Details

Classification
Voluntary Action Indicated (VAI)
End Date
Nov 17, 2010
Fiscal Year
2011
Product Type
Devices
Project Area
Bioresearch Monitoring
Location
Ft Lauderdale, FL (United States)

Additional Details

Clinical Investigator (CI)

Citations

IDCFRDescription
296821 CFR 812.100Investigator non-compliance with agreement/plan/regulations
297021 CFR 812.100Investigator lack of informed consent
302121 CFR 812.150(a)(1)Investigator report of unanticipated adverse effects