FDA inspection

Dr. Reddy's Laboratories (EU) Ltd.: FDA inspection ending Sep 15, 2017

FDA inspection 1036322 · Voluntary Action Indicated (VAI) · Mirfield

Key facts

Inspection ID 1036322
Firm Dr. Reddy's Laboratories (EU) Ltd.
FEI number 3002807544
Address 8QB Steanard Lane, WF14
City Mirfield
Fiscal year 2017
Inspection end date Sep 15, 2017
Classification Voluntary Action Indicated (VAI)
Project area Generic Drug Evaluation
Product type Drugs

At a glance

  • None 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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