FDA inspection
Daito Pharmaceutical Co., Ltd.: FDA inspection ending Nov 10, 2017
FDA inspection 1037107 · Voluntary Action Indicated (VAI) · Toyama
Key facts
| Inspection ID | 1037107 |
|---|---|
| Firm | Daito Pharmaceutical Co., Ltd. |
| FEI number | 3002806779 |
| Address | Daito Pharmaceutical Co., Ltd., 326; Yoka-Machi |
| City | Toyama |
| Fiscal year | 2018 |
| Inspection end date | Nov 10, 2017 |
| 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