Issued to Guangzhou Huli Technology Co., Ltd. dba Fantasy Face. Serious post-market compliance violation.
Issued
March 31, 2026Product
Unapproved New Drugs Sold Over the Internet
Company
Guangzhou Huli Technology Co., Ltd. dba Fantasy Face
Review center
CDERStage
Final Decision
Assyro regulatory brief
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FDA issued a warning letter to Guangzhou Huli Technology Co., Ltd. dba Fantasy Face concerning Unapproved New Drugs Sold Over the Internet. Deterministic full-text screening identifies discussion of Labeling, claims, and misbranding, Unapproved products and premarket authorization. Topic matches are navigation aids, not a legal conclusion; review the exact FDA web letter and any later response or closeout.
Review the exact FDA warning letter, cited violations, requested corrections, and any later response or closeout before assessing current status.
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Serious post-market compliance violation. Public notice requiring prompt remediation. FDA issued this letter on March 31, 2026.
The firm is expected to respond in writing, normally within 15 working days, describing corrective actions and timelines. FDA verifies remediation — often through reinspection — and issues a closeout letter when violations are corrected. Unresolved warning letters can escalate to import alerts, seizure, or injunction.