Skip to content
Assyro AI
US FDA source recordWL · Warning Letter

Glow Medispa, LLC dba Mint Med — FDA Warning Letter

Issued to Glow Medispa, LLC dba Mint Med. Serious post-market compliance violation.

Product

False & Misleading Claims/Misbranded (Telehealth)

Company

Glow Medispa, LLC dba Mint Med

Review center

CDER

Stage

Final Decision

Assyro regulatory brief

Free

Why did Glow Medispa, LLC dba Mint Med receive an FDA warning letter?

Source facts and Assyro context are separated so you can scan the action quickly without treating analysis as an FDA conclusion.

Verify in source

Source facts

FDA issued a warning letter to Glow Medispa, LLC dba Mint Med concerning False & Misleading Claims/Misbranded (Telehealth). Deterministic full-text screening identifies discussion of Labeling, claims, and misbranding. Topic matches are navigation aids, not a legal conclusion; review the exact FDA web letter and any later response or closeout.

Key details in this letter

  • 1Subject: False & Misleading Claims/Misbranded (Telehealth).
  • 2Issuing office: Center for Drug Evaluation and Research (CDER).
  • 3Labeling, claims, and misbranding: 11 source-text matches.
  • 4No closeout letter was listed in the source metadata at refresh time.
Labeling, claims, and misbranding

Suggested next step

Review the exact FDA warning letter, cited violations, requested corrections, and any later response or closeout before assessing current status.

Open the document workspace

Built from structured FDA metadata and deterministic source-text signals. Topic matches are navigation aids, not legal or regulatory conclusions. Verify material decisions against the original FDA document.

FDAHTMLUpdated Jul 30, 2026

FDA source document

Read the full FDA warning letter

FDA publishes this warning letter as a web document.

Open the exact FDA source to read the complete letter and verify its current response or closeout status.

Open source on FDA.gov

Common questions about the Glow Medispa, LLC dba Mint Med warning letter

What does this warning letter mean for Glow Medispa, LLC dba Mint Med?

Serious post-market compliance violation. Public notice requiring prompt remediation. FDA issued this letter on June 8, 2026.

What happens after an FDA warning letter?

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.