FDA Inspection 961294 — Synthon, s.r.o.

Synthon, s.r.o. — FEI 3005212485

The FDA completed an inspection of Synthon, s.r.o. on February 12, 2016 in Blansko. The inspection was classified VAI (Voluntary Action Indicated — objectionable conditions were found but do not meet the threshold for regulatory action). Product area: Drugs.

Inspection Details

Classification
Voluntary Action Indicated (VAI) (VAI)
End Date
February 12, 2016
Fiscal Year
2016
Product Type
Drugs
Project Area
Drug Quality Assurance
Location
Blansko (Czech Republic)