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FDA Inspection 915232 — DeGowin Blood Center

DeGowin Blood Center — FEI 1972918

The FDA completed an inspection of DeGowin Blood Center on February 13, 2015 in Iowa City, IA. 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
February 13, 2015
Fiscal Year
2015
Product Type
Biologics
Project Area
Blood and Blood Products
Location
Iowa City, IA (United States)

Facility

Other inspections at this facility

  • 1259069 (NAI Thu Dec 12 2024 00:00:00 GMT+0000 (Coordinated Universal Time))
  • 1094007 (NAI Thu Jun 06 2019 00:00:00 GMT+0000 (Coordinated Universal Time))
  • 1001567 (NAI Wed Feb 15 2017 00:00:00 GMT+0000 (Coordinated Universal Time))
  • 805206 (VAI Wed Oct 24 2012 00:00:00 GMT+0000 (Coordinated Universal Time))
  • 696431 (NAI Wed Nov 03 2010 00:00:00 GMT+0000 (Coordinated Universal Time))

FDA data resources