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Guangxi Endu High-Tech Co., Ltd

FDA import alert and refusal historyNanning, ChinaFEI 3008094547

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Example subjectGuangxi Endu High-Tech Co., Lt added to Import Alert 16-129 (red list)

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As of October 25, 2026, Guangxi Endu High-Tech Co., Ltd is on the green list of FDA Import Alert 25-05, which exempts its listed products from detention without physical examination under that alert, and has no FDA import refusals recorded since October 2016.

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

Current status

Last import refusal
None since October 2016
Last warning letter
None found
Last inspection
Classified VAI (Voluntary Action Indicated)

Every FDA record for Guangxi Endu High-Tech Co., Ltd

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

2014

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

2013

  1. Import alert listing
    Listed on Import Alert 25-05green listFungi Products Dried
    Source

Questions about Guangxi Endu High-Tech Co., Ltd

Is Guangxi Endu High-Tech Co., Ltd on an FDA import alert?
Yes. As of October 25, 2026, Guangxi Endu High-Tech Co., Ltd is on the green list of FDA Import Alert 25-05, “Dried fungus (mushrooms) from Hong Kong and China: filth”, for fungi products dried; FDA published the listing on March 5, 2013.
Has FDA refused shipments from Guangxi Endu High-Tech Co., Ltd?
No FDA import refusals for Guangxi Endu High-Tech Co., Ltd appear in FDA's refusal data since October 2016, as of October 25, 2026.
When was Guangxi Endu High-Tech Co., Ltd last inspected by FDA?
FDA's most recent inspection of Guangxi Endu High-Tech Co., Ltd with a final classification is dated April 1, 2014 and was classified VAI (Voluntary Action Indicated).
What is Guangxi Endu High-Tech Co., Ltd's FEI number?
Guangxi Endu High-Tech Co., Ltd's FDA Establishment Identifier (FEI) is 3008094547.

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Example subjectGuangxi Endu High-Tech Co., Lt 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.