FDA Inspection 1012792 — Lundbeck Pharmaceuticals Italy S.p.A.

Lundbeck Pharmaceuticals Italy S.p.A. — FEI 3002808449

The FDA completed an inspection of Lundbeck Pharmaceuticals Italy S.p.A. on May 12, 2017 in Padova. 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
May 12, 2017
Fiscal Year
2017
Product Type
Drugs
Project Area
Drug Quality Assurance
Location
Padova (Italy)