FDA Inspection 1191762 — Anna Sediva, M.D., Ph.D.

Anna Sediva, M.D., Ph.D. — FEI 3023715704

The FDA completed an inspection of Anna Sediva, M.D., Ph.D. on November 8, 2022 in Prague 5. 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
November 8, 2022
Fiscal Year
2023
Product Type
Drugs
Project Area
Bioresearch Monitoring
Location
Prague 5 (Czech Republic)

Additional Details

Clinical Investigator (CI)