FDA inspection
Celestica Oregon, LLC.: FDA inspection ending Oct 25, 2019
FDA inspection 1108091 · Voluntary Action Indicated (VAI) · Portland, OR
Key facts
| Inspection ID | 1108091 |
|---|---|
| Firm | Celestica Oregon, LLC. |
| FEI number | 3009039038 |
| Address | 18870 Ne Riverside Pkwy |
| City | Portland |
| State | OR |
| ZIP | 97230 |
| Country | United States |
| Fiscal year | 2020 |
| Inspection end date | Oct 25, 2019 |
| Classification | Voluntary Action Indicated (VAI) |
| Project area | Postmarket Assurance: Devices |
| Product type | Devices |
At a glance
- 1–9 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