FDA inspection
Phibro Suzhou Manufacturing Co., Ltd.: FDA inspection ending May 13, 2016
FDA inspection 971838 · Voluntary Action Indicated (VAI) · Suzhou
Key facts
| Inspection ID | 971838 |
|---|---|
| Firm | Phibro Suzhou Manufacturing Co., Ltd. |
| FEI number | 3012086549 |
| Address | No. 690 Jianlin Road, Huqiu |
| City | Suzhou |
| Country | China |
| Fiscal year | 2016 |
| Inspection end date | May 13, 2016 |
| 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