FDA Warning Letter — LifeServe Blood Center

Case 407983 — FEI 1970355

The FDA took a Warning Letter action against LifeServe Blood Center on August 9, 2013 (Johnston, IA). The action was issued by CBER and concerns biologics products. This facility has 5 or more recent FDA inspections on record.

Action Details

Facility
LifeServe Blood Center
Date
August 9, 2013
Fiscal Year
2013
Product Type
Biologics
Center
CBER
Location
Johnston, IA (United States)