FDA inspection
SOS Hyperlite Limited: FDA inspection ending Aug 12, 2015
FDA inspection 942206 · No Action Indicated (NAI) · Deeside
Key facts
| Inspection ID | 942206 |
|---|---|
| Firm | SOS Hyperlite Limited |
| FEI number | 3010251686 |
| Address | Unit 55, Third Avenue |
| City | Deeside |
| Country | United Kingdom |
| Fiscal year | 2015 |
| Inspection end date | Aug 12, 2015 |
| 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