FDA inspection
Qilu SYNVA Pharmaceutical Co. Ltd: FDA inspection ending Jul 26, 2019
FDA inspection 1098879 · Voluntary Action Indicated (VAI) · Dezhou
Key facts
| Inspection ID | 1098879 |
|---|---|
| Firm | Qilu SYNVA Pharmaceutical Co. Ltd |
| FEI number | 3006385404 |
| Address | 28 Licheng Ave, Linyi County |
| City | Dezhou |
| Country | China |
| Fiscal year | 2019 |
| Inspection end date | Jul 26, 2019 |
| Classification | Voluntary Action Indicated (VAI) |
| Project area | Monitoring of Marketed Animal Drugs, Feed, and Devices |
| Product type | Veterinary |
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