FDA Inspection 1227230 — Unilever Philippines, Inc. - Cavite Factory

Unilever Philippines, Inc. - Cavite Factory — FEI 2000001160

The FDA completed an inspection of Unilever Philippines, Inc. - Cavite Factory on December 13, 2023 in Gen. Trias. The inspection was classified VAI (Voluntary Action Indicated — objectionable conditions were found but do not meet the threshold for regulatory action). Product area: Drugs.

Inspection Details

Classification
Voluntary Action Indicated (VAI) (VAI)
End Date
December 13, 2023
Fiscal Year
2024
Product Type
Drugs
Project Area
Drug Quality Assurance
Location
Gen. Trias (Philippines)