FDA Inspection 1058474 — Zeid Kayali, M.D.

Zeid Kayali, M.D. — FEI 3013967737

The FDA completed an inspection of Zeid Kayali, M.D. on May 24, 2018 in Rialto, CA. The inspection was classified NAI (No Action Indicated — no objectionable conditions or practices were found during the inspection). Product area: Drugs.

Inspection Details

Classification
No Action Indicated (NAI)
End Date
May 24, 2018
Fiscal Year
2018
Product Type
Drugs
Project Area
Bioresearch Monitoring
Location
Rialto, CA (United States)

Additional Details

Clinical Investigator (CI)