FDA inspection
Apixia Inc: FDA inspection ending Feb 14, 2019
FDA inspection 1079324 · Voluntary Action Indicated (VAI) · City Of Industry, CA
Key facts
| Inspection ID | 1079324 |
|---|---|
| Firm | Apixia Inc |
| FEI number | 3008361230 |
| Address | 18688 San Jose Ave Ste 2 |
| City | City Of Industry |
| State | CA |
| ZIP | 91748 |
| Country | United States |
| Fiscal year | 2019 |
| Inspection end date | Feb 14, 2019 |
| Classification | Voluntary Action Indicated (VAI) |
| Project area | Postmarket Assurance: Devices |
| Product type | Devices |
At a glance
- 1–9 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