FDA Inspection 1308158 — Barbara Steinborn, M.D.

Barbara Steinborn, M.D. — FEI 3016446657

The FDA completed an inspection of Barbara Steinborn, M.D. on March 5, 2026 in Poznan. 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
March 5, 2026
Fiscal Year
2026
Product Type
Drugs
Project Area
Bioresearch Monitoring
Location
Poznan (Poland)

Additional Details

Clinical Investigator (CI)