FDA Inspection 815738 — Ibrahim Hanna, MD

Ibrahim Hanna, MD — FEI 3009803623

The FDA completed an inspection of Ibrahim Hanna, MD on Jan 18, 2013 in Birmingham, AL. 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.