FDA inspection

Glenmark Pharmaceuticals Inc., USA: FDA inspection ending Jun 29, 2010

FDA inspection 669685 · Voluntary Action Indicated (VAI) · Elmwood Park, NJ

Key facts

Inspection ID 669685
Firm Glenmark Pharmaceuticals Inc., USA
FEI number 3005658103
Address 750 Corporate Dr
City Elmwood Park
State NJ
ZIP 07407
Country United States
Fiscal year 2010
Inspection end date Jun 29, 2010
Classification Voluntary Action Indicated (VAI)
Project area Bioresearch Monitoring
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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