FDA Inspection 987717 — Hadi Yaziji, MD

Hadi Yaziji, MD — FEI 3012608309

The FDA completed an inspection of Hadi Yaziji, MD on Oct 17, 2016 in Miami, 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). 1 citation was issued during this inspection. Product area: Devices.

Inspection Details

Classification
Voluntary Action Indicated (VAI)
End Date
Oct 17, 2016
Fiscal Year
2017
Product Type
Devices
Project Area
Bioresearch Monitoring
Location
Miami, FL (United States)

Additional Details

Clinical Investigator (CI)

Citations

IDCFRDescription
727021 CFR 56.103(a)IRB review requirement