FDA Warning Letter — Abbott Laboratories

Case 669353 — FEI 1513768

The FDA took a Warning Letter action against Abbott Laboratories on Oct 24, 2023 (Columbus, OH). The action was issued by CBER and concerns biologics products. This facility has 5 or more recent FDA inspections on record.

Action Details

Facility
Abbott Laboratories
Date
Oct 24, 2023
Fiscal Year
2024
Product Type
Biologics
Center
CBER
Location
Columbus, OH (United States)

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