FDA inspection
Asanuma Corporation - Sagamihara Factory: FDA inspection ending Feb 2, 2017
FDA inspection 1002546 · Voluntary Action Indicated (VAI) · Sagamihara
Key facts
| Inspection ID | 1002546 |
|---|---|
| Firm | Asanuma Corporation - Sagamihara Factory |
| FEI number | 3010960168 |
| Address | Sagamihara Factory 1st, 1-14-41 Nishihashimoto; Midori |
| City | Sagamihara |
| Country | Japan |
| Fiscal year | 2017 |
| Inspection end date | Feb 2, 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