FDA inspection

Glenmark Pharmaceuticals Limited: FDA inspection ending May 29, 2015

FDA inspection 929619 · Voluntary Action Indicated (VAI) · Solan

Key facts

Inspection ID 929619
Firm Glenmark Pharmaceuticals Limited
FEI number 3005757050
Address Village Kishanpura, Baddi Nalagarh Road, Baddi
City Solan
Country India
Fiscal year 2015
Inspection end date May 29, 2015
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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