FDA inspection
Guilin Pharmaceutical Co., Ltd.: FDA inspection ending Sep 12, 2008
FDA inspection 543428 · Voluntary Action Indicated (VAI) · Guilin
Key facts
| Inspection ID | 543428 |
|---|---|
| Firm | Guilin Pharmaceutical Co., Ltd. |
| FEI number | 3002807125 |
| Address | No. 43 Qilidian Road |
| City | Guilin |
| Fiscal year | 2008 |
| Inspection end date | Sep 12, 2008 |
| Classification | Voluntary Action Indicated (VAI) |
| 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