FDA Inspection 884632 — EuroAPI Italy SRL

EuroAPI Italy SRL — FEI 3003677892

The FDA completed an inspection of EuroAPI Italy SRL on May 29, 2014 in Brindisi. 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
May 29, 2014
Fiscal Year
2014
Product Type
Drugs
Project Area
Drug Quality Assurance
Location
Brindisi (Italy)