FDA Inspection 1240979 — Latina Pharma S.p.A.

Latina Pharma S.p.A. — FEI 3001229385

The FDA completed an inspection of Latina Pharma S.p.A. on January 19, 2024 in Sermoneta. 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
January 19, 2024
Fiscal Year
2024
Product Type
Drugs
Project Area
Drug Quality Assurance
Location
Sermoneta (Italy)

Additional Details

Mutual Recognition Agreement (MRA)