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US FDA source recordWL · Warning Letter

Viva Raw LLC — FDA Warning Letter

Issued to Viva Raw LLC. Serious post-market compliance violation.

Product

Adulterated Animal Foods/Misbranded

Company

Viva Raw LLC

Review center

CVM

Stage

Final Decision

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Why did Viva Raw LLC 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.

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Source facts

FDA issued a warning letter to Viva Raw LLC concerning Adulterated Animal Foods/Misbranded. Deterministic full-text screening identifies discussion of Quality systems and CAPA. 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: Adulterated Animal Foods/Misbranded.
  • 2Issuing office: Center for Veterinary Medicine.
  • 3Quality systems and CAPA: 1 source-text match.
  • 4No closeout letter was listed in the source metadata at refresh time.
Quality systems and CAPA

Suggested next step

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

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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 Oct 8, 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 Viva Raw LLC warning letter

What does this warning letter mean for Viva Raw LLC?

Serious post-market compliance violation. Public notice requiring prompt remediation. FDA issued this letter on August 5, 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.