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US FDA source recordWL · Warning Letter

Rio Verde Food Service Inc. — FDA Warning Letter

Issued to Rio Verde Food Service Inc.. Serious post-market compliance violation.

Product

Seafood HACCP/CGMP for Foods/Adulterated/Insanitary Conditions

Company

Rio Verde Food Service Inc.

Review center

CFSAN

Stage

Final Decision

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Why did Rio Verde Food Service Inc. receive an FDA warning letter?

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Source facts

FDA issued a warning letter to Rio Verde Food Service Inc. concerning Seafood HACCP/CGMP for Foods/Adulterated/Insanitary Conditions. Deterministic source-metadata screening identifies discussion of 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: Seafood HACCP/CGMP for Foods/Adulterated/Insanitary Conditions.
  • 2Issuing office: Human Foods Program.
  • 3Manufacturing and CGMP controls: 1 source-text match.
  • 4Food safety and supplier verification: 1 source-text match.
Manufacturing 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.

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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 Jul 30, 2026

FDA source document

Read the full FDA warning letter

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Common questions about the Rio Verde Food Service Inc. warning letter

What does this warning letter mean for Rio Verde Food Service Inc.?

Serious post-market compliance violation. Public notice requiring prompt remediation. FDA issued this letter on February 27, 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.