FDA Inspection 1243027 — Martin Kankam

Martin Kankam — FEI 3012716808

The FDA completed an inspection of Martin Kankam on Jun 13, 2024 in Overland Park, KS. 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
Jun 13, 2024
Fiscal Year
2024
Product Type
Drugs
Project Area
Bioresearch Monitoring
Location
Overland Park, KS (United States)

Additional Details

Clinical BA/BE