PMDA inspection

DELPHARM DIJON

PMDA inspection 5130708022766 · France · Suitable

Key facts

Control number 5130708022766
Manufacturing site DELPHARM DIJON
Location 6 boulevard de l'Europe 21800 QUETIGNY, France
Country France
Product type Pharmaceuticals
Application type Regular
Inspection method Remote
Inspection month Sep 1, 2025
Result Suitable
Result notified Sep 10, 2025
PMDA registration AG21000179

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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