FDA inspection

Glenmark Pharmaceuticals Limited: FDA inspection ending Jul 21, 2017

FDA inspection 1025068 · No Action Indicated (NAI) · Aurangabad

Key facts

Inspection ID 1025068
Firm Glenmark Pharmaceuticals Limited
FEI number 3009915929
Address B - 25 Midc Shendra
City Aurangabad
Fiscal year 2017
Inspection end date Jul 21, 2017
Classification No Action Indicated (NAI)
Project area Generic Drug Evaluation
Product type Drugs

At a glance

  • None Citations
  • None 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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