FDA Inspection 1219962 — Solvias AG

Solvias AG — FEI 3008735083

The FDA completed an inspection of Solvias AG on September 1, 2023 in Kaiseraugst. 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
September 1, 2023
Fiscal Year
2023
Product Type
Drugs
Project Area
Bioresearch Monitoring
Location
Kaiseraugst (Switzerland)

Additional Details

Bioanalytical BA/BE