FDA Inspection 1000258 — Glenmark Generics S.A.

Glenmark Generics S.A. — FEI 3009805225

The FDA completed an inspection of Glenmark Generics S.A. on Dec 8, 2016 in Pilar. The inspection was classified OAI (Official Action Indicated — regulatory and/or administrative actions are recommended). Product area: Drugs.

Inspection Details

Classification
Official Action Indicated (OAI)
End Date
Dec 8, 2016
Fiscal Year
2017
Product Type
Drugs
Project Area
Drug Quality Assurance
Location
Pilar (Argentina)

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