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US FDA source recordWL · Warning Letter

Laboratorios Dr. Collado S.A. — FDA Warning Letter

Issued to Laboratorios Dr. Collado S.A.. Serious post-market compliance violation.

Product

CGMP/OTC Finished Pharmaceuticals/Adulterated

Company

Laboratorios Dr. Collado S.A.

Review center

CDER

Stage

Final Decision

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Why did Laboratorios Dr. Collado S.A. receive an FDA warning letter?

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Source facts

FDA issued a warning letter to Laboratorios Dr. Collado S.A. concerning CGMP/OTC Finished Pharmaceuticals/Adulterated. Deterministic full-text screening identifies discussion of Manufacturing and CGMP controls, Labeling, claims, and misbranding, Laboratory controls and testing. 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/OTC Finished Pharmaceuticals/Adulterated.
  • 2Issuing office: Center for Drug Evaluation and Research (CDER).
  • 3Manufacturing and CGMP controls: 11 source-text matches.
  • 4Labeling, claims, and misbranding: 2 source-text matches.
Manufacturing and CGMP controlsLabeling, claims, and misbrandingLaboratory controls and testing

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 Laboratorios Dr. Collado S.A. warning letter

What does this warning letter mean for Laboratorios Dr. Collado S.A.?

Serious post-market compliance violation. Public notice requiring prompt remediation. FDA issued this letter on June 2, 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.