FDA inspection
Kindos Pharmaceuticals Co., Ltd.: FDA inspection ending Jul 30, 2019
FDA inspection 1101348 · No Action Indicated (NAI) · Chengdu
Key facts
| Inspection ID | 1101348 |
|---|---|
| Firm | Kindos Pharmaceuticals Co., Ltd. |
| FEI number | 3008865184 |
| Address | Chengdu Hi-Tech Comprehensive, No. 8-9 Ke Xin Road; Pixian |
| City | Chengdu |
| Country | China |
| Fiscal year | 2019 |
| Inspection end date | Jul 30, 2019 |
| Classification | No Action Indicated (NAI) |
| Project area | Drug Quality Assurance |
| Product type | Drugs |
At a glance
- None Citations
- None Posted citations
- No Warning letter followed
- No 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