FDA inspection

Glenmark Pharmaceuticals Limited: FDA inspection ending May 24, 2018

FDA inspection 1053034 · Voluntary Action Indicated (VAI) · Dhar

Key facts

Inspection ID 1053034
Firm Glenmark Pharmaceuticals Limited
FEI number 3008565058
Address Plot No. 2, Phase-2 Pharma Zone SEZ
City Dhar
Country India
Fiscal year 2018
Inspection end date May 24, 2018
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
  • 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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