Home / Inspections / 920301

FDA Inspection 920301 — LifeServe Blood Center

LifeServe Blood Center — FEI 3011389677

The FDA completed an inspection of LifeServe Blood Center on March 27, 2015 in Sioux City, 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 27, 2015
Fiscal Year
2015
Product Type
Biologics
Project Area
Blood and Blood Products
Location
Sioux City, IA (United States)

Facility

Other inspections at this facility

  • 1315888 (NAI Tue Apr 14 2026 00:00:00 GMT+0000 (Coordinated Universal Time))
  • 1197409 (NAI Wed Feb 01 2023 00:00:00 GMT+0000 (Coordinated Universal Time))
  • 1067221 (NAI Thu Sep 27 2018 00:00:00 GMT+0000 (Coordinated Universal Time))
  • 992546 (NAI Thu Oct 20 2016 00:00:00 GMT+0000 (Coordinated Universal Time))

FDA data resources