FDA inspection
Genentech, Inc.: FDA inspection ending Aug 29, 2012
FDA inspection 796641 · Voluntary Action Indicated (VAI) · South San Francisco, CA
Key facts
| Inspection ID | 796641 |
|---|---|
| Firm | Genentech, Inc. |
| FEI number | 2917293 |
| Address | 1 Dna Way |
| City | South San Francisco |
| State | CA |
| ZIP | 94080 |
| Country | United States |
| Fiscal year | 2012 |
| Inspection end date | Aug 29, 2012 |
| 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
- Yes 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