FDA inspection
Topcon Yamagata Co., Ltd.: FDA inspection ending Feb 20, 2014
FDA inspection 868121 · Voluntary Action Indicated (VAI) · Yamagata
Key facts
| Inspection ID | 868121 |
|---|---|
| Firm | Topcon Yamagata Co., Ltd. |
| FEI number | 3008729548 |
| Address | (Kabu) Topukon'Yamagata, Aza-Ishida 547; Oazaurushiyama; Oazaurushiyama; Oazaurushiyama |
| City | Yamagata |
| Country | Japan |
| Fiscal year | 2014 |
| Inspection end date | Feb 20, 2014 |
| Classification | Voluntary Action Indicated (VAI) |
| Project area | Compliance: Devices |
| Product type | Devices |
At a glance
- 1–9 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