FDA Inspection 1271689 — Synthesia, a.s.

Synthesia, a.s. — FEI 3002675552

The FDA completed an inspection of Synthesia, a.s. on January 18, 2023 in Pardubice 2. 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
January 18, 2023
Fiscal Year
2023
Product Type
Drugs
Project Area
Drug Quality Assurance
Location
Pardubice 2 (Czech Republic)

Additional Details

Mutual Recognition Agreement (MRA)