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Xiamen Kingdomway Group Company

FDA import alert and refusal historyXiamen, ChinaFEI 3008086862

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Example subjectXiamen Kingdomway Group Compan added to Import Alert 16-129 (red list)

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As of October 26, 2026, Xiamen Kingdomway Group Company is not on any FDA import alert in SupplierRadar's records; FDA refused 1 of its shipment line on July 27, 2017, most often for filthy, putrid or decomposed substance (FILTHY).

Data from FDA public records, last checked . Request a correction

Current status

Import alerts
Not listed
Last import refusal
Vitamin, mineral, proteins and unconventional dietary specialities for humans and animals, n.e.c. · FILTHY
Last warning letter
None found
Last inspection
Classified VAI (Voluntary Action Indicated)

Every FDA record for Xiamen Kingdomway Group Company

2 records, newest first. Each line links to the FDA page it came from.

2017

  1. Import refusal
    Refused, Vitamin, mineral, proteins and unconventional dietary specialities for humans and animals, n.e.c.FILTHYEntry UPS-4329826-5
    Source

2014

  1. Inspection
    Inspection classified VAI (Voluntary Action Indicated)Foodborne Biological Hazards
    Source

Refusal charges, in plain English

  • FILTHY1 refused line

    Filthy, putrid or decomposed substance

    The product appeared to consist in whole or in part of a filthy, putrid, or decomposed substance, or to be otherwise unfit for food.

Questions about Xiamen Kingdomway Group Company

Is Xiamen Kingdomway Group Company on an FDA import alert?
No listing for Xiamen Kingdomway Group 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 Xiamen Kingdomway Group Company?
Yes. FDA refused 1 shipment line from Xiamen Kingdomway Group Company on July 27, 2017. The most recent, on July 27, 2017, was vitamin, mineral, proteins and unconventional dietary specialities for humans and animals, n.e.c., charged as FILTHY (filthy, putrid or decomposed substance).
Why did FDA refuse Xiamen Kingdomway Group Company's shipments?
The most frequent charge is FILTHY (filthy, putrid or decomposed substance, 1 line).
When was Xiamen Kingdomway Group Company last inspected by FDA?
FDA's most recent inspection of Xiamen Kingdomway Group Company with a final classification is dated July 29, 2014 and was classified VAI (Voluntary Action Indicated).
What is Xiamen Kingdomway Group Company's FEI number?
Xiamen Kingdomway Group Company's FDA Establishment Identifier (FEI) is 3008086862.

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Example subjectXiamen Kingdomway Group Compan added to Import Alert 16-129 (red list)

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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.