FDA inspection
Zhejiang Raybow Pharmaceutical Co., Ltd.: FDA inspection ending Jul 11, 2019
FDA inspection 1096223 · Voluntary Action Indicated (VAI) · Taizhou
Key facts
| Inspection ID | 1096223 |
|---|---|
| Firm | Zhejiang Raybow Pharmaceutical Co., Ltd. |
| FEI number | 3005842033 |
| Address | 18 Nanyangsan Road, Linhai |
| City | Taizhou |
| Country | China |
| Fiscal year | 2019 |
| Inspection end date | Jul 11, 2019 |
| Classification | Voluntary Action Indicated (VAI) |
| Project area | Drug Quality Assurance |
| Product type | Drugs |
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