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Xian Dadi Phyto Tech Co Inc

FDA import alert and refusal historyXiandang, ChinaFEI 3002732144

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Example subjectXian Dadi Phyto Tech Co In added to Import Alert 16-129 (red list)

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As of October 26, 2026, Xian Dadi Phyto Tech Co Inc (Xiandang, China) is on the red list of FDA Import Alert 99-08 (Processed human and animal foods: pesticides) for panax ginseng powder, published by FDA on September 16, 2009, 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
None on record

Every FDA record for Xian Dadi Phyto Tech Co Inc

1 record, newest first. Each line links to the FDA page it came from.

2009

  1. Import alert listing
    Listed on Import Alert 99-08red listPanax Ginseng Powder
    Source

Questions about Xian Dadi Phyto Tech Co Inc

Is Xian Dadi Phyto Tech Co Inc on an FDA import alert?
Yes. As of October 26, 2026, Xian Dadi Phyto Tech Co Inc is on the red list of FDA Import Alert 99-08, “Processed human and animal foods: pesticides”, for panax ginseng powder; FDA published the listing on September 16, 2009.
Has FDA refused shipments from Xian Dadi Phyto Tech Co Inc?
No FDA import refusals for Xian Dadi Phyto Tech Co Inc appear in FDA's refusal data since October 2016, as of October 26, 2026.
What is Xian Dadi Phyto Tech Co Inc's FEI number?
Xian Dadi Phyto Tech Co Inc's FDA Establishment Identifier (FEI) is 3002732144.
Can shipments from Xian Dadi Phyto Tech Co Inc still enter the U.S.?
Shipments of panax ginseng powder from Xian Dadi Phyto Tech Co Inc can be detained without physical examination under Import Alert 99-08; FDA releases them only if evidence shows they do not have the listed violation. Importers must consider this listing in their FSVP evaluation (21 CFR 1.505).

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Example subjectXian Dadi Phyto Tech Co In 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.