FDA inspection
Acon Biotech (Hangzhou) Co., Ltd.: FDA inspection ending Mar 26, 2005
FDA inspection 377042 · Voluntary Action Indicated (VAI) · Hangzhou
Key facts
| Inspection ID | 377042 |
|---|---|
| Firm | Acon Biotech (Hangzhou) Co., Ltd. |
| FEI number | 3002829675 |
| Address | 398 Tianmushan Road |
| City | Hangzhou |
| Fiscal year | 2005 |
| Inspection end date | Mar 26, 2005 |
| Classification | Voluntary Action Indicated (VAI) |
| Project area | Compliance: Med 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