FDA Inspection 856342 — Wickliffe Pharmaceutical Inc

Wickliffe Pharmaceutical Inc — FEI 3002992930

The FDA completed an inspection of Wickliffe Pharmaceutical Inc on December 3, 2013 in Lexington, KY. The inspection was classified NAI (No Action Indicated — no objectionable conditions were found). Product area: Drugs.

Inspection Details

Classification
No Action Indicated (NAI) (NAI)
End Date
December 3, 2013
Fiscal Year
2014
Product Type
Drugs
Project Area
Drug Quality Assurance
Location
Lexington, KY (United States)