FDA Inspection 920980 — AlloSource

AlloSource — FEI 3003413152

The FDA completed an inspection of AlloSource on April 3, 2015 in Maryland Heights, MO. 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
April 3, 2015
Fiscal Year
2015
Product Type
Biologics
Project Area
Human Cellular, Tissue, and Gene Therapies
Location
Maryland Heights, MO (United States)