FDA inspection
Accriva Diagnostics, Inc.: FDA inspection ending Nov 12, 2010
FDA inspection 702782 · No Action Indicated (NAI) · San Diego, CA
Key facts
| Inspection ID | 702782 |
|---|---|
| Firm | Accriva Diagnostics, Inc. |
| FEI number | 2250033 |
| Address | 6260 Sequence Dr |
| City | San Diego |
| State | CA |
| ZIP | 92121 |
| Country | United States |
| Fiscal year | 2011 |
| Inspection end date | Nov 12, 2010 |
| Classification | No Action Indicated (NAI) |
| Project area | Compliance: 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