FDA Inspection 731125 — EuroAPI Italy SRL

EuroAPI Italy SRL — FEI 3003677892

The FDA completed an inspection of EuroAPI Italy SRL on Mar 17, 2011 in Brindisi. 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
Mar 17, 2011
Fiscal Year
2011
Product Type
Drugs
Project Area
Drug Quality Assurance
Location
Brindisi (Italy)