PMDA registration
BLISSPACK CO., LTD. 2nd Factory
PMDA registration DG10300059 · Republic of Korea
Key facts
| Registration number | DG10300059 |
|---|---|
| Site | BLISSPACK CO., LTD. 2nd Factory |
| Corporation | BLISSPACK CO., LTD. |
| Country | Republic of Korea |
| Type of business | Foreign manufacturers of quasi-drugs |
| Registration categories | Quasi-drugs General |
| Registered | May 18, 2021 |
| Expires | May 17, 2026 |
At a glance
- None PMDA inspections
- Yes 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