FDA Inspection 788969 — Siegfried AG

Siegfried AG — FEI 3002808158

The FDA completed an inspection of Siegfried AG on June 21, 2012 in Zofingen. 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 21, 2012
Fiscal Year
2012
Product Type
Drugs
Project Area
Drug Quality Assurance
Location
Zofingen (Switzerland)