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FDA Inspection 652368 — LifeServe Blood Center

LifeServe Blood Center — FEI 3000209837

The FDA completed an inspection of LifeServe Blood Center on March 19, 2010 in Urbandale, 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
March 19, 2010
Fiscal Year
2010
Product Type
Biologics
Project Area
Blood and Blood Products
Location
Urbandale, IA (United States)

Facility

Other inspections at this facility

  • 1294436 (NAI Wed Dec 03 2025 00:00:00 GMT+0000 (Coordinated Universal Time))
  • 1116972 (NAI Thu Jan 16 2020 00:00:00 GMT+0000 (Coordinated Universal Time))
  • 1038848 (NAI Wed Dec 27 2017 00:00:00 GMT+0000 (Coordinated Universal Time))
  • 946966 (NAI Thu Oct 15 2015 00:00:00 GMT+0000 (Coordinated Universal Time))
  • 880412 (NAI Tue May 20 2014 00:00:00 GMT+0000 (Coordinated Universal Time))

FDA data resources