FDA Inspection 1290486 — Hillel D. Cohen, MD

Hillel D. Cohen, MD — FEI 3040059256

The FDA completed an inspection of Hillel D. Cohen, MD on Oct 31, 2025 in Boca Raton, FL. 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). Product area: Devices.

Inspection Details

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

Additional Details

Clinical Investigator (CI)