FDA Inspection 1038458 — Catalent Argentina S.A.I.C.

Catalent Argentina S.A.I.C. — FEI 3004258511

The FDA completed an inspection of Catalent Argentina S.A.I.C. on Dec 22, 2017 in Buenos Aires. 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.