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US FDA source recordWL · Warning Letter

Hearthy Foods, Inc. — FDA Warning Letter

Issued to Hearthy Foods, Inc.. Serious post-market compliance violation.

Product

CGMP/Dietary Supplement/Adulterated/Misbranded

Company

Hearthy Foods, Inc.

Review center

CFSAN

Stage

Final Decision

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Why did Hearthy Foods, Inc. receive an FDA warning letter?

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Source facts

FDA issued a warning letter to Hearthy Foods, Inc. concerning CGMP/Dietary Supplement/Adulterated/Misbranded. Deterministic full-text screening identifies discussion of Labeling, claims, and misbranding, Manufacturing and CGMP controls, Food safety and supplier verification. 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: CGMP/Dietary Supplement/Adulterated/Misbranded.
  • 2Issuing office: Human Foods Program.
  • 3Labeling, claims, and misbranding: 13 source-text matches.
  • 4Manufacturing and CGMP controls: 8 source-text matches.
Labeling, claims, and misbrandingManufacturing and CGMP controlsFood safety and supplier verification

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.

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Common questions about the Hearthy Foods, Inc. warning letter

What does this warning letter mean for Hearthy Foods, Inc.?

Serious post-market compliance violation. Public notice requiring prompt remediation. FDA issued this letter on February 10, 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.