FDA Inspection 844700 — Latina Pharma S.p.A.

Latina Pharma S.p.A. — FEI 3001229385

The FDA completed an inspection of Latina Pharma S.p.A. on July 24, 2013 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
July 24, 2013
Fiscal Year
2013
Product Type
Drugs
Project Area
Drug Quality Assurance
Location
Sermoneta (Italy)