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Jiangyin TSI Pharmaceutical Company LTD.

FDA import alert and refusal historyJiangyin, ChinaFEI 3004692535

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Example subjectJiangyin TSI Pharmaceutical Company LTD added to Import Alert 16-129 (red list)

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As of October 26, 2026, Jiangyin TSI Pharmaceutical Company LTD. is on the green list of FDA Import Alert 16-02, 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

Import alerts
IA 16-02 · green list
Last import refusal
None since October 2016
Last warning letter
None found
Last inspection
None on record

Every FDA record for Jiangyin TSI Pharmaceutical Company LTD.

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

2009

  1. Import alert listing
    Listed on Import Alert 16-02green listFish Maw, Fishery Products, n.e.c., Ntrl/Artfcl Dried; Shark Fin, Fishery Products, n.e.c., Ntrl/Artfcl Dried; Shark cartilage powder
    Source

Questions about Jiangyin TSI Pharmaceutical Company LTD.

Is Jiangyin TSI Pharmaceutical Company LTD. on an FDA import alert?
Yes. As of October 26, 2026, Jiangyin TSI Pharmaceutical Company LTD. is on the green list of FDA Import Alert 16-02, “Dried shark fins, fish maws and shark cartilage: filth”, for fish maw, fishery products, n.e.c., ntrl/artfcl dried; shark fin, fishery products, n.e.c., ntrl/artfcl dried; shark cartilage powder; FDA published the listing on September 10, 2009.
Has FDA refused shipments from Jiangyin TSI Pharmaceutical Company LTD.?
No FDA import refusals for Jiangyin TSI Pharmaceutical Company LTD. appear in FDA's refusal data since October 2016, as of October 26, 2026.
What is Jiangyin TSI Pharmaceutical Company LTD.'s FEI number?
Jiangyin TSI Pharmaceutical Company LTD.'s FDA Establishment Identifier (FEI) is 3004692535.

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Example subjectJiangyin TSI Pharmaceutical Company LTD 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.