FDA Inspection 1251989 — Rabi Hanna, M.D.

Rabi Hanna, M.D. — FEI 3031927310

The FDA completed an inspection of Rabi Hanna, M.D. on Oct 7, 2024 in Cleveland, OH. 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: Biologics.

Inspection Details

Classification
Voluntary Action Indicated (VAI)
End Date
Oct 7, 2024
Fiscal Year
2025
Product Type
Biologics
Project Area
Bioresearch Monitoring
Location
Cleveland, OH (United States)

Additional Details

Clinical Investigator (CI)

Citations

IDCFRDescription
2272721 CFR 312.64(b)Safety Reports - Serious Events
756021 CFR 312.60FD-1572, protocol compliance

Sources: openFDA, FDA Data Dashboard, FDA.gov. Report a data issue: hello@regdatalab.com.