FDA Warning Letter — Tktx USA

Case 698435 — FEI 3032764588

The FDA took a Warning Letter action against Tktx USA on Feb 25, 2025 (Los Angeles, CA). The action was issued by CDER and concerns drugs products.

Action Details

Facility
Tktx USA
Date
Feb 25, 2025
Fiscal Year
2025
Product Type
Drugs
Center
CDER
Location
Los Angeles, CA (United States)

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