PMDA inspection

Danipharm A/S

PMDA inspection 5130608007825 · Denmark · Suitable

Key facts

Control number 5130608007825
Manufacturing site Danipharm A/S
Location Skalhuse 3, DK-9240 Nibe, Denmark
Country Denmark
Product type Pharmaceuticals
Application type Regular
Inspection method Remote
Inspection month Aug 1, 2024
Result Suitable
Result notified Aug 14, 2024
PMDA registration AG20400013

About PMDA GMP inspections (Japan)

Japan's PMDA conducts GMP and QMS inspections of domestic and foreign manufacturing sites that supply the Japanese market.

Source: Pharmaceuticals and Medical Devices Agency (PMDA), Japan

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