FDA Warning Letter — AriBio H&B

Case 613107 — FEI 3009836687

The FDA took a Warning Letter action against AriBio H&B on October 8, 2021 (Jecheon, South Korea). The action was issued by CDER and concerns drugs products.

Action Details

Facility
AriBio H&B
Date
October 8, 2021
Fiscal Year
2022
Product Type
Drugs
Center
CDER
Location
Jecheon (South Korea)