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FDA Inspection 1022900 — LifeServe Blood Center

LifeServe Blood Center — FEI 1970355

The FDA completed an inspection of LifeServe Blood Center on August 8, 2017 in Johnston, IA. The inspection was classified NAI (No Action Indicated — no objectionable conditions were found). Product area: Biologics.

Inspection Details

Classification
No Action Indicated (NAI) (NAI)
End Date
August 8, 2017
Fiscal Year
2017
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))
  • 979671 (NAI Fri Jul 01 2016 00:00:00 GMT+0000 (Coordinated Universal Time))
  • 943394 (VAI Fri Aug 14 2015 00:00:00 GMT+0000 (Coordinated Universal Time))

Recent compliance actions

FDA data resources