FDA Inspection
Unilever Philippines, Inc. - Cavite FactoryUnilever Philippines, Inc. - Cavite Factory – FDA Inspection, May 10, 2017
Record Details
This FDA Inspection record concerns Unilever Philippines, Inc. - Cavite Factory, with an inspection on May 10, 2017, issued by the Center for Drug Evaluation and Research, covering drugs.
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ID · 115b8d27-11c5-46c8-97fd-19c74bed1e86
Inspection Facts
Voluntary Action Indicated (VAI)
Objectionable conditions were found, but FDA is not prepared to take or recommend regulatory action.
- Inspection number
- 1015345
- FDA center
- Human Drugs
- Project area
- Drug Quality Assurance
- Outcome
- Form 483 issued
Other FDA inspections of Unilever Philippines, Inc. - Cavite Factory
3| Date | Classification | Office | Project area |
|---|---|---|---|
| December 13, 2023 | VAI | Center for Drug Evaluation and Research | Drug Quality Assurance |
| August 16, 2023 | NAI | Center for Food Safety and Applied Nutrition | Food Composition, Standards, Labeling and Econ |
| February 8, 2019 | VAI | Center for Food Safety and Applied Nutrition | Foodborne Biological Hazards |
Other documents for Unilever Philippines, Inc. - Cavite Factory
- FDA Inspection 1227230 - 2023-12-13
- FDA Inspection 1217665 - 2023-08-16
- FDA Inspection 1081211 - 2019-02-08
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