FDA inspection

Glenmark Generics S.A.: FDA inspection ending Dec 8, 2016

FDA inspection 1000258 · Official Action Indicated (OAI) · Pilar

Key facts

Inspection ID 1000258
Firm Glenmark Generics S.A.
FEI number 3009805225
Address Pilar Parque Industrial Calle 9 Ing., Meyer Oks No 593
City Pilar
Country Argentina
Fiscal year 2017
Inspection end date Dec 8, 2016
Classification Official Action Indicated (OAI)
Project area Drug Quality Assurance
Product type Drugs

At a glance

  • 1–9 Citations
  • 1–9 Posted citations
  • No Warning letter followed
  • Yes Form FDA 483 issued
  • No Establishment inspection report (EIR) exists
  • 1–9 Inspections at this FEI

Counts are shown as ranges. Exact figures, trends and every underlying record are available in Orca1.

About FDA inspections

FDA inspections are classified as No Action Indicated (NAI), Voluntary Action Indicated (VAI) or Official Action Indicated (OAI). Inspections of individual clinical investigators are not published here.

Source: U.S. Food and Drug Administration (FDA), inspection classification data

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