FDA Inspection 1206061 — Konrad Rejdak, M.D.

Konrad Rejdak, M.D. — FEI 3025922936

The FDA completed an inspection of Konrad Rejdak, M.D. on May 19, 2023 in Lublin. The inspection was classified OAI (Official Action Indicated — objectionable conditions were found and regulatory action is recommended). 1 citation was issued during this inspection. Product area: Biologics.

Inspection Details

Classification
Official Action Indicated (OAI) (OAI)
End Date
May 19, 2023
Fiscal Year
2023
Product Type
Biologics
Project Area
Bioresearch Monitoring
Location
Lublin (Poland)

Additional Details

Clinical Investigator (CI)

Citations

IDCFRDescription
753021 CFR 312.62(b)Case history records- inadequate or inadequate