FDA inspection
Providien Device Assembly, LLC: FDA inspection ending May 15, 2003
FDA inspection 292252 · No Action Indicated (NAI) · Vista, CA
Key facts
| Inspection ID | 292252 |
|---|---|
| Firm | Providien Device Assembly, LLC |
| FEI number | 1000519289 |
| Address | 2755 Dos Aarons Way Ste B |
| City | Vista |
| State | CA |
| ZIP | 92081-8359 |
| Fiscal year | 2003 |
| Inspection end date | May 15, 2003 |
| 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