FDA Inspection 994677 — AlloSource Inc

AlloSource Inc — FEI 1000305999

The FDA completed an inspection of AlloSource Inc on December 9, 2016 in Cincinnati, OH. 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 9, 2016
Fiscal Year
2017
Product Type
Biologics
Project Area
Human Cellular, Tissue, and Gene Therapies
Location
Cincinnati, OH (United States)