FDA Inspection 803767 — 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 Sep 14, 2012 in Buenos Aires. The inspection was classified NAI (No Action Indicated — no objectionable conditions or practices were found during the inspection). Product area: Drugs.

Inspection details

Classification
No Action Indicated (NAI)
End Date
Sep 14, 2012
Fiscal Year
2012
Product Type
Drugs
Project Area
Drug Quality Assurance
Location
Buenos Aires (Argentina)

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