FDA Inspection 807666 — Willsie, Sandra K

Willsie, Sandra K — FEI 3005234558

The FDA completed an inspection of Willsie, Sandra K on November 8, 2012 in Lenexa, KS. 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
November 8, 2012
Fiscal Year
2013
Product Type
Drugs
Project Area
Bioresearch Monitoring
Location
Lenexa, KS (United States)

Additional Details

Clinical Investigator (CI)