FDA inspection
JMS CO., LTD., Miyoshi Plant: FDA inspection ending Sep 11, 2015
FDA inspection 947326 · Voluntary Action Indicated (VAI) · Miyoshi
Key facts
| Inspection ID | 947326 |
|---|---|
| Firm | JMS CO., LTD., Miyoshi Plant |
| FEI number | 3009249481 |
| Address | Yamaga 350, Shijikkan-Machi |
| City | Miyoshi |
| Country | Japan |
| Fiscal year | 2015 |
| Inspection end date | Sep 11, 2015 |
| Classification | Voluntary Action Indicated (VAI) |
| Project area | Postmarket Assurance: 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