FDA Inspection 1273743 — Viera Donicova, M.D.

Viera Donicova, M.D. — FEI 3035365522

The FDA completed an inspection of Viera Donicova, M.D. on Jun 5, 2025 in Kosice. 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
Jun 5, 2025
Fiscal Year
2025
Product Type
Drugs
Project Area
Bioresearch Monitoring
Location
Kosice (Slovakia)

Additional Details

Clinical Investigator (CI)

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