FDA Inspection 887033 — Synthon Hispania S.L.

Synthon Hispania S.L. — FEI 3004837462

The FDA completed an inspection of Synthon Hispania S.L. on May 23, 2014 in Sant Boi De Llobregat. 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
May 23, 2014
Fiscal Year
2014
Product Type
Drugs
Project Area
Drug Quality Assurance
Location
Sant Boi De Llobregat (Spain)