FDA Warning Letter — Walmart Inc

Case 736557 — FEI 2316750

The FDA took a Warning Letter action against Walmart Inc on Oct 1, 2026 (Bentonville, AR). The action was issued by CDER and concerns drugs products. This facility has 1 recent FDA inspection on record.

Action Details

Facility
Walmart Inc
Date
Oct 1, 2026
Fiscal Year
2027
Product Type
Drugs
Center
CDER
Location
Bentonville, AR (United States)

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