FDA inspection
Kareway Product Inc: FDA inspection ending Mar 28, 2019
FDA inspection 1084225 · Voluntary Action Indicated (VAI) · Compton, CA
Key facts
| Inspection ID | 1084225 |
|---|---|
| Firm | Kareway Product Inc |
| FEI number | 3003867231 |
| Address | 2550 S Dominguez Hills Dr |
| City | Compton |
| State | CA |
| ZIP | 90220 |
| Country | United States |
| Fiscal year | 2019 |
| Inspection end date | Mar 28, 2019 |
| Classification | Voluntary Action Indicated (VAI) |
| Project area | Bioresearch Monitoring |
| Product type | Drugs |
At a glance
- 1–9 Citations
- 1–9 Posted citations
- No Warning letter followed
- Yes Form FDA 483 issued
- Yes 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