FDA Warning Letter — Baxalta US Inc.

Case 119528 — FEI 3000121413

The FDA took a Warning Letter action against Baxalta US Inc. on Aug 3, 2010 (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
Aug 3, 2010
Fiscal Year
2010
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.