FDA Inspection 673196 — Solvias AG

Solvias AG — FEI 3008735083

The FDA completed an inspection of Solvias AG on June 24, 2010 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
June 24, 2010
Fiscal Year
2010
Product Type
Drugs
Project Area
Drug Quality Assurance
Location
Kaiseraugst (Switzerland)