FDA Inspection 986615 — Cassandra E. Curtis, M.D.

Cassandra E. Curtis, M.D. — FEI 3012346039

The FDA completed an inspection of Cassandra E. Curtis, M.D. on September 14, 2016 in Indianapolis, IN. The inspection was classified OAI (Official Action Indicated — objectionable conditions were found and regulatory action is recommended). 8 citations were issued during this inspection. Product area: Drugs.

Inspection Details

Classification
Official Action Indicated (OAI) (OAI)
End Date
September 14, 2016
Fiscal Year
2016
Product Type
Drugs
Project Area
Bioresearch Monitoring
Location
Indianapolis, IN (United States)

Additional Details

Clinical Investigator (CI)

Citations

IDCFRDescription
121 CFR 11Electronic records
749821 CFR 312.66Unanticipated problems
752621 CFR 312.62(a)Accountability records
752721 CFR 312.62(a)Unused drug disposition (investigator)
753021 CFR 312.62(b)Case history records- inadequate or inadequate
754621 CFR 312.64(d)Financial info update
756021 CFR 312.60FD-1572, protocol compliance
756221 CFR 312.60Informed consent