FDA inspection
Guangzhou Berrcom Medical Device Co., Ltd: FDA inspection ending Apr 30, 2015
FDA inspection 926689 · Voluntary Action Indicated (VAI) · Guangzhou
Key facts
| Inspection ID | 926689 |
|---|---|
| Firm | Guangzhou Berrcom Medical Device Co., Ltd |
| FEI number | 3008395508 |
| Address | No 38 Huanzhen Xi Road, Dagang Town |
| City | Guangzhou |
| Country | China |
| Fiscal year | 2015 |
| Inspection end date | Apr 30, 2015 |
| Classification | Voluntary Action Indicated (VAI) |
| Project area | Compliance: 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