FDA Inspection 664318 — AlloSource

AlloSource — FEI 3000215346

The FDA completed an inspection of AlloSource on May 7, 2010 in Centennial, CO. 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: Devices.

Inspection Details

Classification
Voluntary Action Indicated (VAI) (VAI)
End Date
May 7, 2010
Fiscal Year
2010
Product Type
Devices
Project Area
Compliance: Devices
Location
Centennial, CO (United States)

Citations

IDCFRDescription
1247621 CFR 1271.370(b)(1)Identification code affixed