FDA Inspection 1301414 — Gedeon Richter Nyrt.

Gedeon Richter Nyrt. — FEI 3002806761

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

Additional Details

Bioanalytical BA/BE

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