FDA Warning Letter — Supreme Rejuvenation

Case 700749 — FEI 3034929505

The FDA took a Warning Letter action against Supreme Rejuvenation on May 5, 2025 (Houston, TX). The action was issued by CBER and concerns biologics products.

Action Details

Facility
Supreme Rejuvenation
Date
May 5, 2025
Fiscal Year
2025
Product Type
Biologics
Center
CBER
Location
Houston, TX (United States)

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