FDA Inspection 1336632 — 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 Nov 9, 2023 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.

Inspection details

Classification
Voluntary Action Indicated (VAI)
End Date
Nov 9, 2023
Fiscal Year
2024
Product Type
Drugs
Project Area
Drug Quality Assurance
Location
Buenos Aires (Argentina)

Additional details

Mutual Recognition Agreement (MRA)

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