FDA inspection
Sooka Inc: FDA inspection ending Feb 14, 2018
FDA inspection 1050339 · No Action Indicated (NAI) · boca raton, FL
Key facts
| Inspection ID | 1050339 |
|---|---|
| Firm | Sooka Inc |
| FEI number | 3007671445 |
| Address | 578 Washington Blvd Pmb 259 |
| City | boca raton |
| State | FL |
| ZIP | 33432 |
| Country | United States |
| Fiscal year | 2018 |
| Inspection end date | Feb 14, 2018 |
| Classification | No Action Indicated (NAI) |
| Project area | Compliance: Devices |
| Product type | Devices |
At a glance
- None Citations
- None Posted citations
- No Warning letter followed
- No 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