FDA Inspection 1016308 — Saltigo GmbH

Saltigo GmbH — FEI 3010164833

The FDA completed an inspection of Saltigo GmbH on June 8, 2017 in Leverkusen. The inspection was classified NAI (No Action Indicated — no objectionable conditions were found). Product area: Drugs.

Inspection Details

Classification
No Action Indicated (NAI) (NAI)
End Date
June 8, 2017
Fiscal Year
2017
Product Type
Drugs
Project Area
Drug Quality Assurance
Location
Leverkusen (Germany)