FDA inspection
Philips Goldway (Shenzhen) Industrial, Inc.: FDA inspection ending Jul 30, 2015
FDA inspection 942438 · Voluntary Action Indicated (VAI) · Shenzhen
Key facts
| Inspection ID | 942438 |
|---|---|
| Firm | Philips Goldway (Shenzhen) Industrial, Inc. |
| FEI number | 3003687189 |
| Address | No. 2 Keji North 3rd Road, Nanshan District |
| City | Shenzhen |
| Country | China |
| Fiscal year | 2015 |
| Inspection end date | Jul 30, 2015 |
| 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