FDA Inspection 1301414 — Gedeon Richter Nyrt.

Gedeon Richter Nyrt. — FEI 3002806761

The FDA completed an inspection of Gedeon Richter Nyrt. on July 4, 2025 in Budapest. 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
July 4, 2025
Fiscal Year
2025
Product Type
Drugs
Project Area
Bioresearch Monitoring
Location
Budapest (Hungary)

Additional Details

Bioanalytical BA/BE