FDA inspection
Unilever Philippines, Inc. - Cavite Factory: FDA inspection ending May 10, 2017
FDA inspection 1015345 · Voluntary Action Indicated (VAI) · Gen. Trias
Key facts
| Inspection ID | 1015345 |
|---|---|
| Firm | Unilever Philippines, Inc. - Cavite Factory |
| FEI number | 2000001160 |
| Address | 1351 United Nations Avenue |
| City | Gen. Trias |
| Country | Philippines |
| Fiscal year | 2017 |
| Inspection end date | May 10, 2017 |
| Classification | Voluntary Action Indicated (VAI) |
| Project area | Drug Quality Assurance |
| Product type | Drugs |
At a glance
- None Citations
- 1–9 Posted citations
- No Warning letter followed
- Yes Form FDA 483 issued
- No Establishment inspection report (EIR) exists
- 1–9 Inspections at this FEI
Counts are shown as ranges. Exact figures, trends and every underlying record are available in Orca1.
About FDA inspections
FDA inspections are classified as No Action Indicated (NAI), Voluntary Action Indicated (VAI) or Official Action Indicated (OAI). Inspections of individual clinical investigators are not published here.
Source: U.S. Food and Drug Administration (FDA), inspection classification data