FDA Inspection 676571 — Daniel A. Potter, M.D.

Daniel A. Potter, M.D. — FEI 3007671051

The FDA completed an inspection of Daniel A. Potter, M.D. on August 19, 2010 in Laguna Hills, CA. The inspection was classified VAI (Voluntary Action Indicated — objectionable conditions were found but do not meet the threshold for regulatory action). 1 citation was issued during this inspection. Product area: Devices.

Inspection Details

Classification
Voluntary Action Indicated (VAI) (VAI)
End Date
August 19, 2010
Fiscal Year
2010
Product Type
Devices
Project Area
Bioresearch Monitoring
Location
Laguna Hills, CA (United States)

Additional Details

Clinical Investigator (CI)

Citations

IDCFRDescription
1450521 CFR 812.140(a)(3)Investigator's subject records inadequate