FDA inspection
TTY BioPharm Company Ltd (Chungli Factory): FDA inspection ending Mar 18, 2016
FDA inspection 965256 · Voluntary Action Indicated (VAI) · Taoyuan
Key facts
| Inspection ID | 965256 |
|---|---|
| Firm | TTY BioPharm Company Ltd (Chungli Factory) |
| FEI number | 3005054986 |
| Address | Chung-LI Factory, 838 Chung-Hwa Rd., Sec. 1 |
| City | Taoyuan |
| Country | Taiwan |
| Fiscal year | 2016 |
| Inspection end date | Mar 18, 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