FDA inspection
Sichuan Xieli Pharmaceutical Co. Ltd.: FDA inspection ending Jul 1, 2016
FDA inspection 980870 · Voluntary Action Indicated (VAI) · Chengdu
Key facts
| Inspection ID | 980870 |
|---|---|
| Firm | Sichuan Xieli Pharmaceutical Co. Ltd. |
| FEI number | 3007432586 |
| Address | No. 588 Middle Section Of Mudan Avenue, Tianpeng Town |
| City | Chengdu |
| Country | China |
| Fiscal year | 2016 |
| Inspection end date | Jul 1, 2016 |
| 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