FDA Inspection 951967 — Cindy M. Basinski, MD

Cindy M. Basinski, MD — FEI 3011760218

The FDA completed an inspection of Cindy M. Basinski, MD on Dec 3, 2015 in Newburgh, IN. 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). 2 citations were issued during this inspection. Product area: Devices.

Inspection Details

Classification
Voluntary Action Indicated (VAI)
End Date
Dec 3, 2015
Fiscal Year
2016
Product Type
Devices
Project Area
Bioresearch Monitoring
Location
Newburgh, IN (United States)

Additional Details

Clinical Investigator (CI)

Citations

IDCFRDescription
1450521 CFR 812.140(a)(3)Investigator's subject records inadequate
297421 CFR 812.110(b)Investigator non-compliance with agreement/plan/regulations