FDA inspection
Genentech, Inc.: FDA inspection ending Mar 12, 2024
FDA inspection 1233203 · Voluntary Action Indicated (VAI) · South San Francisco, CA
Key facts
| Inspection ID | 1233203 |
|---|---|
| Firm | Genentech, Inc. |
| FEI number | 2917293 |
| Address | 600 E Grand Ave Rm 40-4c |
| City | South San Francisco |
| State | CA |
| ZIP | 94080 |
| Country | United States |
| Fiscal year | 2024 |
| Inspection end date | Mar 12, 2024 |
| 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
- No Establishment inspection report (EIR) exists
- 10–99 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