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FDA Inspection 620060 — American Donor Services

American Donor Services — FEI 3003947376

The FDA completed an inspection of American Donor Services on September 29, 2009 in Cottage Grove, MN. 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
September 29, 2009
Fiscal Year
2009
Product Type
Biologics
Project Area
Human Cellular, Tissue, and Gene Therapies
Location
Cottage Grove, MN (United States)

Facility

Other inspections at this facility

  • 1172621 (NAI Thu May 26 2022 00:00:00 GMT+0000 (Coordinated Universal Time))
  • 1024626 (NAI Tue Aug 22 2017 00:00:00 GMT+0000 (Coordinated Universal Time))
  • 910710 (NAI Fri Jan 09 2015 00:00:00 GMT+0000 (Coordinated Universal Time))
  • 809135 (NAI Mon Dec 03 2012 00:00:00 GMT+0000 (Coordinated Universal Time))
  • 730554 (NAI Mon Jun 13 2011 00:00:00 GMT+0000 (Coordinated Universal Time))

FDA data resources