FDA Inspection 861128 — Viacord LLC

Viacord LLC — FEI 3003978223

The FDA completed an inspection of Viacord LLC on December 18, 2013 in Hebron, KY. The inspection was classified NAI (No Action Indicated — no objectionable conditions were found). Product area: Biologics.

Inspection Details

Classification
No Action Indicated (NAI) (NAI)
End Date
December 18, 2013
Fiscal Year
2014
Product Type
Biologics
Project Area
Human Cellular, Tissue, and Gene Therapies
Location
Hebron, KY (United States)