FDA Inspection 1015345 — Unilever Philippines, Inc. - Cavite Factory
The FDA completed an inspection of Unilever Philippines, Inc. - Cavite Factory on May 10, 2017 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: Drugs.
Inspection details
- Classification
- Voluntary Action Indicated (VAI)
- End Date
- May 10, 2017
- Fiscal Year
- 2017
- Product Type
- Drugs
- Project Area
- Drug Quality Assurance
- Location
- Gen. Trias (Philippines)