FDA inspection
Xinxiang Tuoxin Pharmaceutical Co. Ltd: FDA inspection ending Jun 6, 2019
FDA inspection 1095514 · Official Action Indicated (OAI) · Xinxiang
Key facts
| Inspection ID | 1095514 |
|---|---|
| Firm | Xinxiang Tuoxin Pharmaceutical Co. Ltd |
| FEI number | 3008259785 |
| Address | Muye And Deyuan Road Cross Street |
| City | Xinxiang |
| Country | China |
| Fiscal year | 2019 |
| Inspection end date | Jun 6, 2019 |
| Classification | Official Action Indicated (OAI) |
| 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