FDA inspection

Glenmark Pharmaceuticals Limited: FDA inspection ending Mar 15, 2019

FDA inspection 1082656 · Voluntary Action Indicated (VAI) · Colvale

Key facts

Inspection ID 1082656
Firm Glenmark Pharmaceuticals Limited
FEI number 3004672766
Address Plot No. S-7, Colvale Industrial Estate
City Colvale
Country India
Fiscal year 2019
Inspection end date Mar 15, 2019
Classification Voluntary Action Indicated (VAI)
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
  • 10–99 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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