FDA inspection

Unilever Manufacturing (US), Inc.: FDA inspection ending Oct 12, 2004

FDA inspection 349060 · No Action Indicated (NAI) · Jonesboro, AR

Key facts

Inspection ID 349060
Firm Unilever Manufacturing (US), Inc.
FEI number 3006642851
Address 2407 Quality Way
City Jonesboro
State AR
ZIP 72401-9264
Fiscal year 2005
Inspection end date Oct 12, 2004
Classification No Action Indicated (NAI)
Project area Colors and Cosmetics Technology
Product type Food/Cosmetics

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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