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Ue Choon Lee Co.,Ltd

FDA import alert and refusal historyRat Burana, ThailandFEI 2000038611

Recorded by FDA as UE CHOON LEE CO.,LTD

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Example subjectUe Choon Lee Co.,Lt added to Import Alert 16-129 (red list)

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As of October 26, 2026, Ue Choon Lee Co.,Ltd (Rat Burana, Thailand) is on the red list of FDA Import Alert 16-120 (Seafood from processors not in compliance with HACCP) for shrimp paste products, published by FDA on March 4, 2019, and has 9 FDA import refusals recorded since October 2016.

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

Current status

Last import refusal
Shrimp paste, fishery products, n.e.c. · MFRHACCP
Last warning letter
None found
Last inspection
Classified OAI (Official Action Indicated)

Every FDA record for Ue Choon Lee Co.,Ltd

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

2024

  1. Import refusal
    Refused, Shrimp paste, fishery products, n.e.c.MFRHACCPEntry KM6-3635541-4
    Source

2019

  1. Import refusal
    Refused, 3 lines in one entry: Shrimp paste, fishery products, n.e.c.MFRHACCPEntry HK1-1901820-6Show 3 lines
    • Refused, Shrimp paste, fishery products, n.e.c.MFRHACCPEntry HK1-1901820-6Source
    • Refused, Shrimp paste, fishery products, n.e.c.MFRHACCPEntry HK1-1901820-6Source
    • Refused, Shrimp paste, fishery products, n.e.c.MFRHACCPEntry HK1-1901820-6Source
    Source
  2. Import refusal
    Refused, 2 lines in one entry: Shrimp paste, fishery products, n.e.c.MFRHACCPEntry J34-0087101-1Show 2 lines
    • Refused, Shrimp paste, fishery products, n.e.c.MFRHACCPEntry J34-0087101-1Source
    • Refused, Shrimp paste, fishery products, n.e.c.MFRHACCPEntry J34-0087101-1Source
    Source
  3. Import refusal
    Refused, 3 lines in one entry: Shrimp paste, fishery products, n.e.c.MFRHACCPEntry 349-1009416-7Show 3 lines
    • Refused, Shrimp paste, fishery products, n.e.c.MFRHACCPEntry 349-1009416-7Source
    • Refused, Shrimp paste, fishery products, n.e.c.MFRHACCPEntry 349-1009416-7Source
    • Refused, Shrimp paste, fishery products, n.e.c.MFRHACCPEntry 349-1009416-7Source
    Source
  4. Import alert listing
    Listed on Import Alert 16-120red listShrimp Paste Products
    Source

2018

  1. Inspection
    Inspection classified OAI (Official Action Indicated)Foodborne Biological Hazards
    Source

Refusal charges, in plain English

  • MFRHACCP9 refused lines

    Seafood HACCP requirements not met

    The seafood appeared to have been processed without meeting the seafood HACCP requirements in 21 CFR 123.6(a) and 123.8(a), so it is treated as prepared under insanitary conditions.

Questions about Ue Choon Lee Co.,Ltd

Is Ue Choon Lee Co.,Ltd on an FDA import alert?
Yes. As of October 26, 2026, Ue Choon Lee Co.,Ltd is on the red list of FDA Import Alert 16-120, “Seafood from processors not in compliance with HACCP”, for shrimp paste products; FDA published the listing on March 4, 2019.
Has FDA refused shipments from Ue Choon Lee Co.,Ltd?
Yes. FDA refused 9 shipment lines from Ue Choon Lee Co.,Ltd between July 3, 2019 and October 30, 2024. The most recent, on October 30, 2024, was shrimp paste, fishery products, n.e.c., charged as MFRHACCP (seafood haccp requirements not met).
Why did FDA refuse Ue Choon Lee Co.,Ltd's shipments?
The most frequent charge is MFRHACCP (seafood haccp requirements not met, 9 lines).
When was Ue Choon Lee Co.,Ltd last inspected by FDA?
FDA's most recent inspection of Ue Choon Lee Co.,Ltd with a final classification is dated August 15, 2018 and was classified OAI (Official Action Indicated).
What is Ue Choon Lee Co.,Ltd's FEI number?
Ue Choon Lee Co.,Ltd's FDA Establishment Identifier (FEI) is 2000038611.
Can shipments from Ue Choon Lee Co.,Ltd still enter the U.S.?
Shipments of shrimp paste products from Ue Choon Lee Co.,Ltd can be detained without physical examination under Import Alert 16-120; 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 subjectUe Choon Lee 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.