FDA inspection

Glenmark Pharmaceuticals Inc., USA: FDA inspection ending May 7, 2020

FDA inspection 1124105 · No Action Indicated (NAI) · Monroe, NC

Key facts

Inspection ID 1124105
Firm Glenmark Pharmaceuticals Inc., USA
FEI number 3011585599
Address 4147 Goldmine Rd
City Monroe
State NC
ZIP 28110-7759
Fiscal year 2020
Inspection end date May 7, 2020
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

Browse all FDA inspections