FDA Inspection 989402 — AlloSource

AlloSource — FEI 3003413152

The FDA completed an inspection of AlloSource on October 24, 2016 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
October 24, 2016
Fiscal Year
2017
Product Type
Biologics
Project Area
Human Cellular, Tissue, and Gene Therapies
Location
Maryland Heights, MO (United States)