FDA inspection
Providien Device Assembly, LLC: FDA inspection ending Nov 3, 2010
FDA inspection 696342 · No Action Indicated (NAI) · Vista, CA
Key facts
| Inspection ID | 696342 |
|---|---|
| Firm | Providien Device Assembly, LLC |
| FEI number | 1000519289 |
| Address | 2755 Dos Aarons Way Ste B |
| City | Vista |
| State | CA |
| ZIP | 92081 |
| Country | United States |
| Fiscal year | 2011 |
| Inspection end date | Nov 3, 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