FDA Inspection 1340372 — LifeServe Blood Center

LifeServe Blood Center — FEI 3018921483

The FDA completed an inspection of LifeServe Blood Center on Sep 29, 2026 in Ankeny, IA. The inspection was classified NAI (No Action Indicated — no objectionable conditions or practices were found during the inspection). Product area: Biologics.

Inspection Details

Classification
No Action Indicated (NAI)
End Date
Sep 29, 2026
Fiscal Year
2026
Product Type
Biologics
Project Area
Blood and Blood Products
Location
Ankeny, IA (United States)

Sources: openFDA, FDA Data Dashboard, FDA.gov. Report a data issue: hello@regdatalab.com.