FDA Inspection 645825 — EuroAPI Hungary Ltd.

EuroAPI Hungary Ltd. — FEI 3002806675

The FDA completed an inspection of EuroAPI Hungary Ltd. on February 4, 2010 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
February 4, 2010
Fiscal Year
2010
Product Type
Drugs
Project Area
Drug Quality Assurance
Location
Budapest (Hungary)