FDA Inspection 1290486 — Hillel D. Cohen, MD

Hillel D. Cohen, MD — FEI 3040059256

The FDA completed an inspection of Hillel D. Cohen, MD on October 31, 2025 in Boca Raton, FL. The inspection was classified VAI (Voluntary Action Indicated — objectionable conditions were found but do not meet the threshold for regulatory action). Product area: Devices.

Inspection Details

Classification
Voluntary Action Indicated (VAI) (VAI)
End Date
October 31, 2025
Fiscal Year
2026
Product Type
Devices
Project Area
Bioresearch Monitoring
Location
Boca Raton, FL (United States)

Additional Details

Clinical Investigator (CI)