FDA inspection
Accriva Diagnostics, Inc.: FDA inspection ending Jan 20, 2000
FDA inspection 10528 · No Action Indicated (NAI) · San Diego, CA
Key facts
| Inspection ID | 10528 |
|---|---|
| Firm | Accriva Diagnostics, Inc. |
| FEI number | 2250033 |
| Address | 6260 Sequence Dr |
| City | San Diego |
| State | CA |
| ZIP | 92121-4358 |
| Fiscal year | 2000 |
| Inspection end date | Jan 20, 2000 |
| Classification | No Action Indicated (NAI) |
| Project area | Compliance: Med Devices |
| Product type | Devices |
At a glance
- None Citations
- None 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