FDA inspection
Spiracle Technology: FDA inspection ending Mar 23, 2017
FDA inspection 1019791 · Voluntary Action Indicated (VAI) · Los Alamitos, CA
Key facts
| Inspection ID | 1019791 |
|---|---|
| Firm | Spiracle Technology |
| FEI number | 3000204983 |
| Address | 10601 Calle Lee Ste 190 |
| City | Los Alamitos |
| State | CA |
| ZIP | 90720-6788 |
| Fiscal year | 2017 |
| Inspection end date | Mar 23, 2017 |
| Classification | Voluntary Action Indicated (VAI) |
| Project area | Compliance: Medical 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