FDA Warning Letter — IDO PHARM

Case 723449 — FEI 3017021001

The FDA took a Warning Letter action against IDO PHARM on May 4, 2026 (Ansan, South Korea). The action was issued by CDER and concerns drugs products. This facility has 1 recent FDA inspection on record.

Action Details

Facility
IDO PHARM
Date
May 4, 2026
Fiscal Year
2026
Product Type
Drugs
Center
CDER
Location
Ansan (South Korea)