FDA Inspection 1296692 — IDO PHARM

IDO PHARM — FEI 3017021001

The FDA completed an inspection of IDO PHARM on Nov 13, 2025 in Ansan. The inspection was classified OAI (Official Action Indicated — regulatory and/or administrative actions are recommended). Product area: Drugs.

Inspection Details

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

Sources: openFDA, FDA Data Dashboard, FDA.gov. Report a data issue: hello@regdatalab.com.