FDA inspection

Unilever Manufacturing (US), Inc.: FDA inspection ending Jul 10, 2015

FDA inspection 942794 · Voluntary Action Indicated (VAI) · Jonesboro, AR

Key facts

Inspection ID 942794
Firm Unilever Manufacturing (US), Inc.
FEI number 3006642851
Address 2407 Quality Way
City Jonesboro
State AR
ZIP 72401
Country United States
Fiscal year 2015
Inspection end date Jul 10, 2015
Classification Voluntary Action Indicated (VAI)
Project area Drug Quality Assurance
Product type Drugs

At a glance

  • 1–9 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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