FDA Inspection 1255310 — Tadeusz Debniak, MD

Tadeusz Debniak, MD — FEI 3031806450

The FDA completed an inspection of Tadeusz Debniak, MD on Nov 7, 2024 in Szczecin. 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
Nov 7, 2024
Fiscal Year
2025
Product Type
Drugs
Project Area
Bioresearch Monitoring
Location
Szczecin (Poland)

Additional Details

Clinical Investigator (CI)

Sources: openFDA, FDA Data Dashboard, FDA.gov. Report a data issue: hello@regdatalab.com.