FDA Inspection 1194879 — Dottikon Exclusive Synthesis AG

Dottikon Exclusive Synthesis AG — FEI 3002806909

The FDA completed an inspection of Dottikon Exclusive Synthesis AG on December 16, 2022 in Dottikon. 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
December 16, 2022
Fiscal Year
2023
Product Type
Drugs
Project Area
Drug Quality Assurance
Location
Dottikon (Switzerland)