PMDA registration
Sakura Finetek USA, Inc.
PMDA registration EG30400030 · USA
Key facts
| Registration number | EG30400030 |
|---|---|
| Site | Sakura Finetek USA, Inc. |
| Corporation | Sakura Finetek USA, Inc. |
| Country | USA |
| Type of business | Foreign manufacturers of in vitro diagnostic drugs |
| Registration categories | In vitro diagnostic drug registration |
| Registered | Jul 12, 2023 |
| Expires | Jul 11, 2028 |
At a glance
- None PMDA inspections
- No Registration expired
- No Registration abolished
Counts are shown as ranges. Exact figures, trends and every underlying record are available in Orca1.
About PMDA registered foreign manufacturers (Japan)
Foreign manufacturers of drugs and medical devices supplied to Japan must be registered (accredited) with the Ministry of Health, Labour and Welfare through the PMDA.
Source: Pharmaceuticals and Medical Devices Agency (PMDA), Japan