# Unilever Philippines, Inc. - Cavite Factory – FDA Inspection, May 10, 2017

Source: https://www.keypedia.com/records/fda_inspections/unilever-philippines-inc-cavite-factory/115b8d27-11c5-46c8-97fd-19c74bed1e86
Source feed: FDA_Inspections

> FDA inspection 1015345 of Unilever Philippines, Inc. - Cavite Factory, May 10, 2017. Classification: Voluntary Action Indicated (VAI). Form 483 issued. 3 other FDA inspections on record for this company.

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## Details

- Record Type: FDA Inspection
- Inspection ID: 1015345
- Company Name: Unilever Philippines, Inc. - Cavite Factory
- Inspection Date: 2017-05-10
- Classification: Voluntary Action Indicated (VAI)
- Classification Code: VAI
- Project Area: Drug Quality Assurance
- Product Type: Drugs
- Center: Human Drugs
- Office Name: Center for Drug Evaluation and Research
- Citation Count: 0

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## Related Officers

- [Company Rep](https://www.keypedia.com/people/michael-l-casner/a0f35f37-4795-4edf-a9f6-a447d64c0fd4)

Company: https://www.keypedia.com/companies/unilever-philippines-inc-cavite-factory/38935d26-4a75-403a-82af-91eb2082abd4

Office: https://www.keypedia.com/offices/center-for-drug-evaluation-and-research/cd980d74-1cbf-4226-ba9a-9045324c236c