FDA inspection
TTY Biopharm Company Limited Lioudu Factory: FDA inspection ending Aug 30, 2022
FDA inspection 1179269 · Voluntary Action Indicated (VAI) · Keelung City
Key facts
| Inspection ID | 1179269 |
|---|---|
| Firm | TTY Biopharm Company Limited Lioudu Factory |
| FEI number | 3015497585 |
| Address | Qidu District, No. 5 Gongjian W. Rd.; Qidu Dist. |
| City | Keelung City |
| Fiscal year | 2022 |
| Inspection end date | Aug 30, 2022 |
| Classification | Voluntary Action Indicated (VAI) |
| Project area | Generic Drug Evaluation |
| Product type | Drugs |
At a glance
- 1–9 Citations
- 1–9 Posted citations
- No Warning letter followed
- Yes Form FDA 483 issued
- Yes 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