FDA Warning Letter — Bloodworks

Case 394402 — FEI 3071347

The FDA took a Warning Letter action against Bloodworks on April 16, 2013 (Seattle, WA). The action was issued by CBER and concerns biologics products. This facility has 5 or more recent FDA inspections on record.

Action Details

Facility
Bloodworks
Date
April 16, 2013
Fiscal Year
2013
Product Type
Biologics
Center
CBER
Location
Seattle, WA (United States)