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FDA Inspection 943394 — LifeServe Blood Center

LifeServe Blood Center — FEI 1970355

The FDA completed an inspection of LifeServe Blood Center on August 14, 2015 in Johnston, 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
August 14, 2015
Fiscal Year
2015
Product Type
Biologics
Project Area
Blood and Blood Products
Location
Johnston, IA (United States)

Facility

Other inspections at this facility

  • 1257768 (NAI Fri Nov 22 2024 00:00:00 GMT+0000 (Coordinated Universal Time))
  • 1105239 (NAI Wed Sep 18 2019 00:00:00 GMT+0000 (Coordinated Universal Time))
  • 1068080 (NAI Thu Aug 23 2018 00:00:00 GMT+0000 (Coordinated Universal Time))
  • 1022900 (NAI Tue Aug 08 2017 00:00:00 GMT+0000 (Coordinated Universal Time))
  • 979671 (NAI Fri Jul 01 2016 00:00:00 GMT+0000 (Coordinated Universal Time))

Recent compliance actions

FDA data resources