FDA Inspection 707726 — Egis Pharmaceuticals PLC

Egis Pharmaceuticals PLC — FEI 3002806880

The FDA completed an inspection of Egis Pharmaceuticals PLC on Jan 28, 2011 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
Jan 28, 2011
Fiscal Year
2011
Product Type
Drugs
Project Area
Drug Quality Assurance
Location
Budapest (Hungary)