FDA Inspection 1092876 — Kazimierz Kuliczkowski, M.D.

Kazimierz Kuliczkowski, M.D. — FEI 3011759280

The FDA completed an inspection of Kazimierz Kuliczkowski, M.D. on May 16, 2019 in Wroclaw. 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
May 16, 2019
Fiscal Year
2019
Product Type
Drugs
Project Area
Bioresearch Monitoring
Location
Wroclaw (Poland)

Additional Details

Clinical Investigator (CI)