FDA Inspection 889637 — Siegfried St. Vulbas SAS

Siegfried St. Vulbas SAS — FEI 3002807787

The FDA completed an inspection of Siegfried St. Vulbas SAS on December 18, 2013 in Saint-Vulbas. 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 18, 2013
Fiscal Year
2014
Product Type
Drugs
Project Area
Drug Quality Assurance
Location
Saint-Vulbas (France)