FDA Inspection 856350 — AlloSource

AlloSource — FEI 3003413152

The FDA completed an inspection of AlloSource on November 22, 2013 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
November 22, 2013
Fiscal Year
2014
Product Type
Biologics
Project Area
Human Cellular, Tissue, and Gene Therapies
Location
Maryland Heights, MO (United States)