FDA inspection

Glenmark Pharmaceuticals Limited: FDA inspection ending May 30, 2014

FDA inspection 885332 · No Action Indicated (NAI) · Colvale

Key facts

Inspection ID 885332
Firm Glenmark Pharmaceuticals Limited
FEI number 3004672766
Address Plot No S - 7, Colvale Industrial Estate
City Colvale
Country India
Fiscal year 2014
Inspection end date May 30, 2014
Classification No Action Indicated (NAI)
Project area Drug Quality Assurance
Product type Drugs

At a glance

  • None Citations
  • None Posted citations
  • No Warning letter followed
  • No 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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