FDA inspection
Zhejiang Huayi Pharmaceutical Co., Ltd.: FDA inspection ending Mar 16, 2018
FDA inspection 1050113 · Voluntary Action Indicated (VAI) · Jinhua
Key facts
| Inspection ID | 1050113 |
|---|---|
| Firm | Zhejiang Huayi Pharmaceutical Co., Ltd. |
| FEI number | 3003657871 |
| Address | Shuangfeng Rd, No. 15 Fotangzhen Zhong; Yiwu |
| City | Jinhua |
| Country | China |
| Fiscal year | 2018 |
| Inspection end date | Mar 16, 2018 |
| 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