FDA Inspection 1081211 — Unilever Philippines, Inc. - Cavite Factory

Unilever Philippines, Inc. - Cavite Factory — FEI 2000001160

The FDA completed an inspection of Unilever Philippines, Inc. - Cavite Factory on Feb 8, 2019 in Gen. Trias. The inspection was classified VAI (Voluntary Action Indicated — objectionable conditions or practices were found, but the agency is not prepared to take or recommend any administrative or regulatory action). Product area: Food/Cosmetics.

Inspection details

Classification
Voluntary Action Indicated (VAI)
End Date
Feb 8, 2019
Fiscal Year
2019
Product Type
Food/Cosmetics
Project Area
Foodborne Biological Hazards
Location
Gen. Trias (Philippines)

Sources: openFDA, FDA Data Dashboard, FDA.gov. Report a data issue: hello@regdatalab.com.