FDA Warning Letter — Baxalta US Inc.

Case 52964 — FEI 3000121413

The FDA took a Warning Letter action against Baxalta US Inc. on Apr 14, 2009 (Westlake Village, CA). The action was issued by CBER and concerns biologics products. This facility has 5 or more recent FDA inspections on record.

Action Details

Facility
Baxalta US Inc.
Date
Apr 14, 2009
Fiscal Year
2009
Product Type
Biologics
Center
CBER
Location
Westlake Village, CA (United States)

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