FDA Inspection 771277 — AlloSource

AlloSource — FEI 3003657798

The FDA completed an inspection of AlloSource on March 12, 2012 in Chicago, IL. The inspection was classified VAI (Voluntary Action Indicated — objectionable conditions were found but do not meet the threshold for regulatory action). 1 citation was issued during this inspection. Product area: Biologics.

Inspection Details

Classification
Voluntary Action Indicated (VAI) (VAI)
End Date
March 12, 2012
Fiscal Year
2012
Product Type
Biologics
Project Area
Human Cellular, Tissue, and Gene Therapies
Location
Chicago, IL (United States)

Citations

IDCFRDescription
1241121 CFR 1271.260(a)Contamination, mix ups, improper release