FDA Inspection 1267207 — HENRY KANAREK, M.D.

HENRY KANAREK, M.D. — FEI 3026585057

The FDA completed an inspection of HENRY KANAREK, M.D. on March 26, 2025 in Overland Park, KS. The inspection was classified NAI (No Action Indicated — no objectionable conditions were found). Product area: Biologics.

Inspection Details

Classification
No Action Indicated (NAI) (NAI)
End Date
March 26, 2025
Fiscal Year
2025
Product Type
Biologics
Project Area
Bioresearch Monitoring
Location
Overland Park, KS (United States)

Additional Details

Clinical Investigator (CI)