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Ah Yee Taung Co Ltd

FDA import alert and refusal historyAungmyaythat San, MyanmarFEI 3024099446

Recorded by FDA as AH YEE TAUNG CO LTD

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Example subjectAh Yee Taung Co Lt added to Import Alert 16-129 (red list)

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As of October 26, 2026, Ah Yee Taung Co Ltd is not on any FDA import alert in SupplierRadar's records; FDA refused 6 of its shipment lines between April 16, 2024 and September 9, 2025, most often for nutrition information missing from label (NUTRIT LBL).

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

Current status

Import alerts
Not listed
Last import refusal
Mustard greens, dried or paste · NO ENGLISH
Last warning letter
None found
Last inspection
None on record

Every FDA record for Ah Yee Taung Co Ltd

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

2025

  1. Import refusal
    Refused, 3 lines in one entry: Mustard greens, dried or paste; Other fruits and fruit products, other fruit juices or concentrates, n.e.c.NO ENGLISHNEEDS FCENO PROCESSUNSAFE COLEntry 609-0657250-2Show 3 lines
    Source

2024

  1. Import refusal
    Refused, 3 lines in one entry: Anchovy; Curry powder, liquid, without salt and 1 moreFILTHYNUTRIT LBLNEEDS FCENO PROCESSEntry 202-2976775-9Show 3 lines
    Source

Refusal charges, in plain English

  • NUTRIT LBL5 refused lines

    Nutrition information missing from label

    The label or labeling appeared not to carry the nutrition information that U.S. law requires for the food.

  • UNSAFE COL3 refused lines

    Color additive unsafe under section 721

    The product appeared to be, or to contain, a color additive that is unsafe within the meaning of section 721(a) of the FD&C Act, the section that governs which color additives may be used and how.

  • NEEDS FCE2 refused lines

    Processor not registered for canned or acidified foods

    The manufacturer appeared not to be registered with FDA as a low-acid canned food or acidified food processor, as 21 CFR 108.25 and 108.35 require.

  • NO ENGLISH2 refused lines

    Required label information not in English

    Information that must appear on the label appeared not to be given in English, or not to be repeated in every language used on the label.

  • NO PROCESS2 refused lines

    No scheduled process filed

    The manufacturer appeared not to have filed a scheduled process with FDA, which 21 CFR Part 108 requires for low-acid canned and acidified foods, so the product is treated as made under insanitary conditions.

  • FILTHY1 refused line

    Filthy, putrid or decomposed substance

    The product appeared to consist in whole or in part of a filthy, putrid, or decomposed substance, or to be otherwise unfit for food.

  • JUICE %1 refused line

    Juice percentage not declared

    The product is presented as a beverage containing fruit or vegetable juice and the label appeared not to state the total percentage of juice on the information panel.

  • LACKS N/C1 refused line

    Net quantity statement missing

    The packaged food appeared not to carry an accurate statement of the quantity of contents, such as net weight, measure, or count, on its label.

Questions about Ah Yee Taung Co Ltd

Is Ah Yee Taung Co Ltd on an FDA import alert?
No listing for Ah Yee Taung Co Ltd appears in the FDA import alerts SupplierRadar checked on October 26, 2026. Country-wide alerts may still apply to its products; see the Myanmar page.
Has FDA refused shipments from Ah Yee Taung Co Ltd?
Yes. FDA refused 6 shipment lines from Ah Yee Taung Co Ltd between April 16, 2024 and September 9, 2025. The most recent, on September 9, 2025, was mustard greens, dried or paste, charged as NO ENGLISH (required label information not in english).
Why did FDA refuse Ah Yee Taung Co Ltd's shipments?
The most frequent charges are NUTRIT LBL (nutrition information missing from label, 5 lines) and UNSAFE COL (color additive unsafe under section 721, 3 lines).
What is Ah Yee Taung Co Ltd's FEI number?
Ah Yee Taung Co Ltd's FDA Establishment Identifier (FEI) is 3024099446.

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Example subjectAh Yee Taung 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.