FDA Inspection 1081211 — Unilever Philippines, Inc. - Cavite Factory
The FDA completed an inspection of Unilever Philippines, Inc. - Cavite Factory on February 8, 2019 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: Food/Cosmetics.
Inspection Details
- Classification
- Voluntary Action Indicated (VAI) (VAI)
- End Date
- February 8, 2019
- Fiscal Year
- 2019
- Product Type
- Food/Cosmetics
- Project Area
- Foodborne Biological Hazards
- Location
- Gen. Trias (Philippines)