FDA Inspection 620109 — Cellumed Co., Ltd.

Cellumed Co., Ltd. — FEI 3006404440

The FDA completed an inspection of Cellumed Co., Ltd. on Sep 18, 2009 in Seoul. The inspection was classified VAI (Voluntary Action Indicated — objectionable conditions or practices were found, but the agency is not prepared to take or recommend any administrative or regulatory action). Product area: Biologics.

Inspection Details

Classification
Voluntary Action Indicated (VAI)
End Date
Sep 18, 2009
Fiscal Year
2009
Product Type
Biologics
Project Area
Human Cellular, Tissue, and Gene Therapies
Location
Seoul (Korea (the Republic of))