FDA Inspection 604425 — Dakhil, Dr Shaker

Dakhil, Dr Shaker — FEI 3007381886

The FDA completed an inspection of Dakhil, Dr Shaker on July 22, 2009 in Wichita, KS. The inspection was classified VAI (Voluntary Action Indicated — objectionable conditions were found but do not meet the threshold for regulatory action). Product area: Drugs.

Inspection Details

Classification
Voluntary Action Indicated (VAI) (VAI)
End Date
July 22, 2009
Fiscal Year
2009
Product Type
Drugs
Project Area
Bioresearch Monitoring
Location
Wichita, KS (United States)

Additional Details

Clinical Investigator (CI)