FDA Inspection 948704 — Ziad F. Issa, MD

Ziad F. Issa, MD — FEI 3011931469

The FDA completed an inspection of Ziad F. Issa, MD on Nov 20, 2015 in Springfield, IL. The inspection was classified NAI (No Action Indicated — no objectionable conditions or practices were found during the inspection). Product area: Devices.

Inspection Details

Classification
No Action Indicated (NAI)
End Date
Nov 20, 2015
Fiscal Year
2016
Product Type
Devices
Project Area
Bioresearch Monitoring
Location
Springfield, IL (United States)

Additional Details

Clinical Investigator (CI)