FDA inspection
Ashitaka Factory of Terumo Corporation: FDA inspection ending Oct 28, 2004
FDA inspection 352689 · No Action Indicated (NAI) · Fujinomiya
Key facts
| Inspection ID | 352689 |
|---|---|
| Firm | Ashitaka Factory of Terumo Corporation |
| FEI number | 3002808327 |
| Address | 150, Maimaigi-Cho |
| City | Fujinomiya |
| Fiscal year | 2005 |
| Inspection end date | Oct 28, 2004 |
| Classification | No Action Indicated (NAI) |
| Project area | Compliance: Med Devices |
| Product type | Devices |
At a glance
- None Citations
- None 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