FDA inspection

Estee Lauder N.V.: FDA inspection ending Sep 15, 2017

FDA inspection 1030311 · Voluntary Action Indicated (VAI) · Oevel

Key facts

Inspection ID 1030311
Firm Estee Lauder N.V.
FEI number 1000224360
Address Nijverheidsstraat 15
City Oevel
Country Belgium
Fiscal year 2017
Inspection end date Sep 15, 2017
Classification Voluntary Action Indicated (VAI)
Project area Drug Quality Assurance
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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