FDA Inspection 1247299 — Celltrion Pharm, Inc.

Celltrion Pharm, Inc. — FEI 3012279978

The FDA completed an inspection of Celltrion Pharm, Inc. on July 23, 2024 in Cheongju. The inspection was classified VAI (Voluntary Action Indicated — objectionable conditions were found but do not meet the threshold for regulatory action). Product area: Drugs.

Inspection Details

Classification
Voluntary Action Indicated (VAI) (VAI)
End Date
July 23, 2024
Fiscal Year
2024
Product Type
Drugs
Project Area
Drug Quality Assurance
Location
Cheongju (Korea (the Republic of))