FDA inspection

Auronext Pharma: FDA inspection ending Aug 5, 2016

FDA inspection 981299 · Voluntary Action Indicated (VAI) · Bhiwadi

Key facts

Inspection ID 981299
Firm Auronext Pharma
FEI number 3009883410
Address A-1128, Riico Industrial Area, Phase -Iii, District Alwar
City Bhiwadi
Fiscal year 2016
Inspection end date Aug 5, 2016
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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