FDA Inspection 1278330 — Egis Pharmaceuticals PLC

Egis Pharmaceuticals PLC — FEI 3002806880

The FDA completed an inspection of Egis Pharmaceuticals PLC on Jul 5, 2024 in Budapest. The inspection was classified VAI (Voluntary Action Indicated — objectionable conditions or practices were found, but the agency is not prepared to take or recommend any administrative or regulatory action). Product area: Drugs.

Inspection Details

Classification
Voluntary Action Indicated (VAI)
End Date
Jul 5, 2024
Fiscal Year
2024
Product Type
Drugs
Project Area
Drug Quality Assurance
Location
Budapest (Hungary)

Additional Details

Mutual Recognition Agreement (MRA)