FDA Inspection 1285910 — Frantisek Duska, M.D.

Frantisek Duska, M.D. — FEI 3036583868

The FDA completed an inspection of Frantisek Duska, M.D. on August 22, 2025 in Prague. The inspection was classified VAI (Voluntary Action Indicated — objectionable conditions were found but do not meet the threshold for regulatory action). Product area: Biologics.

Inspection Details

Classification
Voluntary Action Indicated (VAI) (VAI)
End Date
August 22, 2025
Fiscal Year
2025
Product Type
Biologics
Project Area
Bioresearch Monitoring
Location
Prague (Czech Republic)

Additional Details

Clinical Investigator (CI)