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FDA Inspection 929703 — AlloSource

AlloSource — FEI 3000215346

The FDA completed an inspection of AlloSource on June 11, 2015 in Centennial, CO. The inspection was classified VAI (Voluntary Action Indicated — objectionable conditions were found but do not meet the threshold for regulatory action). Product area: Biologics.

Inspection Details

Classification
Voluntary Action Indicated (VAI) (VAI)
End Date
June 11, 2015
Fiscal Year
2015
Product Type
Biologics
Project Area
Human Cellular, Tissue, and Gene Therapies
Location
Centennial, CO (United States)

Facility

Other inspections at this facility

  • 1201259 (NAI Thu Mar 30 2023 00:00:00 GMT+0000 (Coordinated Universal Time))
  • 1175639 (NAI Wed Jul 27 2022 00:00:00 GMT+0000 (Coordinated Universal Time))
  • 1074854 (NAI Tue Dec 18 2018 00:00:00 GMT+0000 (Coordinated Universal Time))
  • 1010063 (VAI Thu Feb 09 2017 00:00:00 GMT+0000 (Coordinated Universal Time))
  • 781336 (VAI Mon Jun 04 2012 00:00:00 GMT+0000 (Coordinated Universal Time))

FDA data resources