FDA inspection
Sunlit Fluo & Chemical Co., Ltd. Chung-Li Factory: FDA inspection ending Aug 26, 2016
FDA inspection 987395 · Voluntary Action Indicated (VAI) · Taoyuan City
Key facts
| Inspection ID | 987395 |
|---|---|
| Firm | Sunlit Fluo & Chemical Co., Ltd. Chung-Li Factory |
| FEI number | 3003034746 |
| Address | Chung LI Industry Park, NO. 39 Dongyuan Rd.; Zhongli City |
| City | Taoyuan City |
| Country | Taiwan |
| Fiscal year | 2016 |
| Inspection end date | Aug 26, 2016 |
| 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