FDA inspection
TTY Biopharm Company Limited Lioudu Factory: FDA inspection ending Apr 22, 2025
FDA inspection 1270648 · Voluntary Action Indicated (VAI) · Keelung City
Key facts
| Inspection ID | 1270648 |
|---|---|
| Firm | TTY Biopharm Company Limited Lioudu Factory |
| FEI number | 3015497585 |
| Address | Qidu District, No. 5 Gongjian West Rd.; Qidu Dist. |
| City | Keelung City |
| Country | Taiwan |
| Fiscal year | 2025 |
| Inspection end date | Apr 22, 2025 |
| 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