FDA inspection

Unilever Philippines, Inc. - Cavite Factory: FDA inspection ending Feb 8, 2019

FDA inspection 1081211 · Voluntary Action Indicated (VAI) · Gen. Trias

Key facts

Inspection ID 1081211
Firm Unilever Philippines, Inc. - Cavite Factory
FEI number 2000001160
Address Gateway Business Park, General Trias
City Gen. Trias
Country Philippines
Fiscal year 2019
Inspection end date Feb 8, 2019
Classification Voluntary Action Indicated (VAI)
Project area Foodborne Biological Hazards
Product type Food/Cosmetics

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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