FDA inspection
Isorx Corp: FDA inspection ending Sep 18, 2019
FDA inspection 1102533 · Voluntary Action Indicated (VAI) · Richmond, CA
Key facts
| Inspection ID | 1102533 |
|---|---|
| Firm | Isorx Corp |
| FEI number | 3006624492 |
| Address | 845 Marina Bay Pkwy Ste 9 |
| City | Richmond |
| State | CA |
| ZIP | 94804 |
| Country | United States |
| Fiscal year | 2019 |
| Inspection end date | Sep 18, 2019 |
| 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