FDA Warning Letter — Celltrion Inc.

Case 534262 — FEI 3005241015

The FDA took a Warning Letter action against Celltrion Inc. on Jan 29, 2018 (Yeonsu, South Korea). The action was issued by CDER and concerns drugs products. This facility has 5 or more recent FDA inspections on record.

Action details

Facility
Celltrion Inc.
Date
Jan 29, 2018
Fiscal Year
2018
Product Type
Drugs
Center
CDER
Location
Yeonsu (South Korea)

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