FDA inspection
Solaris Medical Technology, Inc.: FDA inspection ending May 24, 2012
FDA inspection 790019 · Voluntary Action Indicated (VAI) · Shenzhen
Key facts
| Inspection ID | 790019 |
|---|---|
| Firm | Solaris Medical Technology, Inc. |
| FEI number | 3006552505 |
| Address | Yanshan Rd, Shekou # 401, 18 Zhongjian Industrial Building One; Nanshan District |
| City | Shenzhen |
| Country | China |
| Fiscal year | 2012 |
| Inspection end date | May 24, 2012 |
| Classification | Voluntary Action Indicated (VAI) |
| Project area | Compliance: 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