FDA inspection
Mikasa X-Ray Co., Ltd.: FDA inspection ending Mar 10, 2017
FDA inspection 1008403 · Voluntary Action Indicated (VAI) · Bunkyo
Key facts
| Inspection ID | 1008403 |
|---|---|
| Firm | Mikasa X-Ray Co., Ltd. |
| FEI number | 3002807605 |
| Address | 5 Chome 10-5, Koishikawa |
| City | Bunkyo |
| Country | Japan |
| Fiscal year | 2017 |
| Inspection end date | Mar 10, 2017 |
| 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