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US FDA source recordWL · Warning Letter

Active Cosmetics Manufacturing Inc. — FDA Warning Letter

Issued to Active Cosmetics Manufacturing Inc.. Serious post-market compliance violation.

Product

CGMP/Finished Pharmaceuticals/Adulterated

Company

Active Cosmetics Manufacturing Inc.

Review center

CDER

Stage

Final Decision

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Why did Active Cosmetics Manufacturing Inc. receive an FDA warning letter?

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Source facts

FDA issued a warning letter to Active Cosmetics Manufacturing Inc. concerning CGMP/Finished Pharmaceuticals/Adulterated. Deterministic full-text screening identifies discussion of Laboratory controls and testing, Manufacturing and CGMP controls, Quality systems and CAPA, 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: CGMP/Finished Pharmaceuticals/Adulterated.
  • 2Issuing office: Center for Drug Evaluation and Research (CDER).
  • 3Laboratory controls and testing: 15 source-text matches.
  • 4Manufacturing and CGMP controls: 12 source-text matches.
Laboratory controls and testingManufacturing and CGMP controlsQuality systems and CAPALabeling, 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.

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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 Active Cosmetics Manufacturing Inc. warning letter

What does this warning letter mean for Active Cosmetics Manufacturing Inc.?

Serious post-market compliance violation. Public notice requiring prompt remediation. FDA issued this letter on April 22, 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.