FDA Inspection 1134974 — Synthon, s.r.o.

Synthon, s.r.o. — FEI 3005212485

The FDA completed an inspection of Synthon, s.r.o. on May 16, 2019 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
May 16, 2019
Fiscal Year
2019
Product Type
Drugs
Project Area
Drug Quality Assurance
Location
Blansko (Czech Republic)

Additional Details

Mutual Recognition Agreement (MRA)