FDA Inspection 1296692 — IDO PHARM

IDO PHARM — FEI 3017021001

The FDA completed an inspection of IDO PHARM on November 13, 2025 in Ansan. The inspection was classified OAI (Official Action Indicated — objectionable conditions were found and regulatory action is recommended). Product area: Drugs.

Inspection Details

Classification
Official Action Indicated (OAI) (OAI)
End Date
November 13, 2025
Fiscal Year
2026
Product Type
Drugs
Project Area
Drug Quality Assurance
Location
Ansan (Korea (the Republic of))