FDA Inspection
Unilever Philippines, Inc. - Cavite FactoryUnilever Philippines, Inc. - Cavite Factory – FDA Inspection, Dec 13, 2023
Record Details
This FDA Inspection record concerns Unilever Philippines, Inc. - Cavite Factory, with an inspection on December 13, 2023, issued by the Center for Drug Evaluation and Research, covering drugs.
View Company Profile
ID · 19d56a4d-9945-46b9-b339-cd7e9aa14ed7
Inspection Facts
Voluntary Action Indicated (VAI)
Objectionable conditions were found, but FDA is not prepared to take or recommend regulatory action.
- Inspection number
- 1227230
- 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 |
|---|---|---|---|
| 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 |
| May 10, 2017 | VAI | Center for Drug Evaluation and Research | Drug Quality Assurance |
Other documents for Unilever Philippines, Inc. - Cavite Factory
- FDA Inspection 1217665 - 2023-08-16
- FDA Inspection 1081211 - 2019-02-08
- FDA Inspection 1015345 - 2017-05-10
Document or profile
One record shows the event. A profile shows the pattern.
Buy this document for the source file and details behind this single event.
Choose full profile access to connect related records, sites, people, citations, and enforcement history in one view.