FDA Inspection 1046602 — Marta Banach, M.D.

Marta Banach, M.D. — FEI 3014126608

The FDA completed an inspection of Marta Banach, M.D. on Mar 2, 2018 in Cracow. 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
Mar 2, 2018
Fiscal Year
2018
Product Type
Drugs
Project Area
Bioresearch Monitoring
Location
Cracow (Poland)

Additional Details

Clinical Investigator (CI)

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