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Jiang Men Cutlery Manufactory

FDA import alert and refusal historyJiang Men, ChinaFEI 1000291348

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Example subjectJiang Men Cutlery Manufactor added to Import Alert 16-129 (red list)

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As of October 26, 2026, Jiang Men Cutlery Manufactory (Jiang Men, China) is on the red list of FDA Import Alert 45-02 (Foods with illegal or undeclared colors) for shrimp/prawn crackers, published by FDA on September 18, 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 Jiang Men Cutlery Manufactory

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

2009

  1. Import alert listing
    Listed on Import Alert 45-02red listShrimp/Prawn Crackers
    Source

Questions about Jiang Men Cutlery Manufactory

Is Jiang Men Cutlery Manufactory on an FDA import alert?
Yes. As of October 26, 2026, Jiang Men Cutlery Manufactory is on the red list of FDA Import Alert 45-02, “Foods with illegal or undeclared colors”, for shrimp/prawn crackers; FDA published the listing on September 18, 2009.
Has FDA refused shipments from Jiang Men Cutlery Manufactory?
No FDA import refusals for Jiang Men Cutlery Manufactory appear in FDA's refusal data since October 2016, as of October 26, 2026.
What is Jiang Men Cutlery Manufactory's FEI number?
Jiang Men Cutlery Manufactory's FDA Establishment Identifier (FEI) is 1000291348.
Can shipments from Jiang Men Cutlery Manufactory still enter the U.S.?
Shipments of shrimp/prawn crackers from Jiang Men Cutlery Manufactory can be detained without physical examination under Import Alert 45-02; 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 subjectJiang Men Cutlery Manufactor 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.