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Xi An TECHTEAM TECHNOLOGY INDUSTRY (GROUP) CO.LTD.

FDA import alert and refusal historyXian, ChinaFEI 3004663338

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Example subjectXi An TECHTEAM TECHNOLOGY INDUSTRY (GROUP) CO.LTD added to Import Alert 16-129 (red list)

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As of October 26, 2026, Xi An TECHTEAM TECHNOLOGY INDUSTRY (GROUP) CO.LTD. (Xian, China) is on the red list of FDA Import Alert 99-08 (Processed human and animal foods: pesticides) for dried goji berries (wolfberries), 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

Import alerts
IA 99-08 · red list
Last import refusal
None since October 2016
Last warning letter
None found
Last inspection
None on record

Every FDA record for Xi An TECHTEAM TECHNOLOGY INDUSTRY (GROUP) CO.LTD.

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 listDried Goji Berries (Wolfberries)
    Source

Questions about Xi An TECHTEAM TECHNOLOGY INDUSTRY (GROUP) CO.LTD.

Is Xi An TECHTEAM TECHNOLOGY INDUSTRY (GROUP) CO.LTD. on an FDA import alert?
Yes. As of October 26, 2026, Xi An TECHTEAM TECHNOLOGY INDUSTRY (GROUP) CO.LTD. is on the red list of FDA Import Alert 99-08, “Processed human and animal foods: pesticides”, for dried goji berries (wolfberries); FDA published the listing on September 16, 2009.
Has FDA refused shipments from Xi An TECHTEAM TECHNOLOGY INDUSTRY (GROUP) CO.LTD.?
No FDA import refusals for Xi An TECHTEAM TECHNOLOGY INDUSTRY (GROUP) CO.LTD. appear in FDA's refusal data since October 2016, as of October 26, 2026.
What is Xi An TECHTEAM TECHNOLOGY INDUSTRY (GROUP) CO.LTD.'s FEI number?
Xi An TECHTEAM TECHNOLOGY INDUSTRY (GROUP) CO.LTD.'s FDA Establishment Identifier (FEI) is 3004663338.
Can shipments from Xi An TECHTEAM TECHNOLOGY INDUSTRY (GROUP) CO.LTD. still enter the U.S.?
Shipments of dried goji berries (wolfberries) from Xi An TECHTEAM TECHNOLOGY INDUSTRY (GROUP) CO.LTD. 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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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.