FDA inspection
Alere San Diego, Inc.: FDA inspection ending Mar 15, 2000
FDA inspection 16460 · Voluntary Action Indicated (VAI) · San Diego, CA
Key facts
| Inspection ID | 16460 |
|---|---|
| Firm | Alere San Diego, Inc. |
| FEI number | 1000125596 |
| Address | 9975 Summers Ridge Rd |
| City | San Diego |
| State | CA |
| ZIP | 92121-2997 |
| Fiscal year | 2000 |
| Inspection end date | Mar 15, 2000 |
| Classification | Voluntary Action Indicated (VAI) |
| Project area | Product Evaluation: Med Devices |
| Product type | Devices |
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