FDA inspection
Shenzhen Techdow Pharmaceutical Co., Ltd.: FDA inspection ending Mar 27, 2018
FDA inspection 1050101 · Voluntary Action Indicated (VAI) · Shenzhen
Key facts
| Inspection ID | 1050101 |
|---|---|
| Firm | Shenzhen Techdow Pharmaceutical Co., Ltd. |
| FEI number | 3005599762 |
| Address | 19 Gaoxinzhongyi Road, Nanshan |
| City | Shenzhen |
| Fiscal year | 2018 |
| Inspection end date | Mar 27, 2018 |
| Classification | Voluntary Action Indicated (VAI) |
| Project area | Generic Drug Evaluation |
| 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