FDA Inspection 1018753 — Latina Pharma S.P.A.

Latina Pharma S.P.A. — FEI 3001229385

The FDA completed an inspection of Latina Pharma S.P.A. on Apr 21, 2017 in Sermoneta. The inspection was classified VAI (Voluntary Action Indicated — objectionable conditions or practices were found, but the agency is not prepared to take or recommend any administrative or regulatory action). Product area: Drugs.

Inspection details

Classification
Voluntary Action Indicated (VAI)
End Date
Apr 21, 2017
Fiscal Year
2017
Product Type
Drugs
Project Area
Drug Quality Assurance
Location
Sermoneta (Italy)

Sources: openFDA, FDA Data Dashboard, FDA.gov. Report a data issue: hello@regdatalab.com.