FDA Inspection 1240749 — Krzysztof Szymanowski, M.D.

Krzysztof Szymanowski, M.D. — FEI 3030358734

The FDA completed an inspection of Krzysztof Szymanowski, M.D. on May 17, 2024 in Dopiewo. 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
May 17, 2024
Fiscal Year
2024
Product Type
Drugs
Project Area
Bioresearch Monitoring
Location
Dopiewo (Poland)

Additional Details

Clinical Investigator (CI)