FDA Inspection 955993 — Benzy Padanilam, M.D.

Benzy Padanilam, M.D. — FEI 3011750813

The FDA completed an inspection of Benzy Padanilam, M.D. on Jan 15, 2016 in Indianapolis, 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
Jan 15, 2016
Fiscal Year
2016
Product Type
Devices
Project Area
Bioresearch Monitoring
Location
Indianapolis, IN (United States)

Additional Details

Clinical Investigator (CI)

Citations

IDCFRDescription
1450521 CFR 812.140(a)(3)Investigator's subject records inadequate
296821 CFR 812.100Investigator non-compliance with agreement/plan/regulations