Herb Dimension Limited Company
FDA import alert and refusal historyBeijing, ChinaFEI 3015256441
As of October 26, 2026, Herb Dimension Limited Company is not on any FDA import alert in SupplierRadar's records; FDA refused 2 of its shipment lines on November 10, 2021, most often for poisonous or deleterious substance (POISONOUS).
Data from FDA public records, last checked . Request a correction
Current status
- Import alerts
- Not listed
- Last import refusal
- Angelica (herbals & botanical teas) · POISONOUS
- Last warning letter
- None found
- Last inspection
- None on record
Every FDA record for Herb Dimension Limited Company
2 records, newest first. Each line links to the FDA page it came from.
2021
- Import refusalSource
Refused, 2 lines in one entry: Angelica (herbals & botanical teas); Ginkgo biloba (herbal & botanical teas)POISONOUSEntry 156-0145618-7Show 2 linesHide lines
Refusal charges, in plain English
- POISONOUS2 refused lines
Poisonous or deleterious substance
The product appeared to bear or contain a poisonous or deleterious substance which may render it injurious to health.
Questions about Herb Dimension Limited Company
- Is Herb Dimension Limited Company on an FDA import alert?
- No listing for Herb Dimension Limited Company appears in the FDA import alerts SupplierRadar checked on October 26, 2026. Country-wide alerts may still apply to its products; see the China page.
- Has FDA refused shipments from Herb Dimension Limited Company?
- Yes. FDA refused 2 shipment lines from Herb Dimension Limited Company on November 10, 2021. The most recent, on November 10, 2021, was angelica (herbals & botanical teas), charged as POISONOUS (poisonous or deleterious substance).
- Why did FDA refuse Herb Dimension Limited Company's shipments?
- The most frequent charge is POISONOUS (poisonous or deleterious substance, 2 lines).
- What is Herb Dimension Limited Company's FEI number?
- Herb Dimension Limited Company's FDA Establishment Identifier (FEI) is 3015256441.
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SupplierRadar is not affiliated with the U.S. Food and Drug Administration. Data comes from public FDA records and may contain errors. This is not legal advice; importers remain responsible for their supplier evaluations.