FDA Inspection 934776 — Saltigo GmbH

Saltigo GmbH — FEI 3010164833

The FDA completed an inspection of Saltigo GmbH on June 3, 2015 in Leverkusen. 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 3, 2015
Fiscal Year
2015
Product Type
Drugs
Project Area
Drug Quality Assurance
Location
Leverkusen (Germany)