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US FDA source recordWL · Warning Letter

Yangzhou H&R Plastic Daily Chemical Co., Ltd. — FDA Warning Letter

Issued to Yangzhou H&R Plastic Daily Chemical Co., Ltd.. Serious post-market compliance violation.

Product

CGMP/Finished Pharmaceuticals/Adulterated

Company

Yangzhou H&R Plastic Daily Chemical Co., Ltd.

Review center

CDER

Stage

Final Decision

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Why did Yangzhou H&R Plastic Daily Chemical Co., Ltd. receive an FDA warning letter?

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Source facts

FDA issued a warning letter to Yangzhou H&R Plastic Daily Chemical Co., Ltd. concerning CGMP/Finished Pharmaceuticals/Adulterated. Deterministic full-text screening identifies discussion of Manufacturing and CGMP controls, Laboratory controls and testing, 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).
  • 3Manufacturing and CGMP controls: 21 source-text matches.
  • 4Laboratory controls and testing: 1 source-text match.
Manufacturing and CGMP controlsLaboratory controls and testingQuality 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 Yangzhou H&R Plastic Daily Chemical Co., Ltd. warning letter

What does this warning letter mean for Yangzhou H&R Plastic Daily Chemical Co., Ltd.?

Serious post-market compliance violation. Public notice requiring prompt remediation. FDA issued this letter on March 18, 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.