FDA Inspection 805197 — Synthon, s.r.o.
The FDA completed an inspection of Synthon, s.r.o. on October 25, 2012 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
- October 25, 2012
- Fiscal Year
- 2013
- Product Type
- Drugs
- Project Area
- Drug Quality Assurance
- Location
- Blansko (Czech Republic)