FDA Inspection 920301 — LifeServe Blood Center

LifeServe Blood Center — FEI 3011389677

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

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