FDA Inspection 1056604 — Alfasigma S.p.A.

Alfasigma S.p.A. — FEI 3002808171

The FDA completed an inspection of Alfasigma S.p.A. on June 21, 2018 in Pomezia. 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, 2018
Fiscal Year
2018
Product Type
Drugs
Project Area
Drug Quality Assurance
Location
Pomezia (Italy)