SupplierRadar

Asisa Trakulwatt Anasin

FDA import alert and refusal historyTak, ThailandFEI 3013253409

Recorded by FDA as ASISA TRAKULWATT ANASIN

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Example subjectAsisa Trakulwatt Anasi added to Import Alert 16-129 (red list)

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As of October 26, 2026, Asisa Trakulwatt Anasin is not on any FDA import alert in SupplierRadar's records; FDA refused 8 of its shipment lines between February 27, 2018 and January 21, 2020, most often for fair packaging and labeling act (LABELING).

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

Current status

Import alerts
Not listed
Last import refusal
Betel nut (herbal and botanicals, not teas ii) · POISONOUS
Last warning letter
None found
Last inspection
None on record

Every FDA record for Asisa Trakulwatt Anasin

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

2020

  1. Import refusal
    Refused, Betel nut (herbal and botanicals, not teas ii)POISONOUSLACKS FIRMEntry SCS-8059039-2
    Source
  2. Import refusal
    Refused, Betel leaf (herbal and botanical (not teas) ii (continued))POISONOUSEntry SCS-8098169-0
    Source
  3. Import refusal
    Refused, Betel leaf (herbal and botanical (not teas) ii (continued))LACKS FIRMLABELINGNUTRIT LBLEntry SCS-8159795-8
    Source
  4. Import refusal
    Refused, Betel leaf (herbal and botanical (not teas) ii (continued))LACKS FIRMLABELINGNUTRIT LBLEntry SCS-8178693-2
    Source

2018

  1. Import refusal
    Refused, Fish paste, fishery products, n.e.c.MFRHACCPLABELINGEntry AEK-4387381-6
    Source
  2. Import refusal
    Refused, 3 lines in one entry: Fish paste, fishery products, n.e.c.; Turmeric, ground, cracked (spice) and 1 moreFILTHYLABELINGEntry AEK-4269757-0Show 3 lines
    Source

Refusal charges, in plain English

  • LABELING6 refused lines

    Fair Packaging and Labeling Act

    The package appeared not to meet the Fair Packaging and Labeling Act because of the placement, form, or contents of a required label statement.

  • FILTHY3 refused lines

    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.

  • LACKS FIRM3 refused lines

    Manufacturer name and address missing

    The packaged product's label appeared not to show the name and place of business of the manufacturer, packer, or distributor.

  • NUTRIT LBL2 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.

  • POISONOUS2 refused lines

    Poisonous or deleterious substance

    The product appeared to bear or contain a poisonous or deleterious substance which may render it injurious to health.

  • MFRHACCP1 refused line

    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 Asisa Trakulwatt Anasin

Is Asisa Trakulwatt Anasin on an FDA import alert?
No listing for Asisa Trakulwatt Anasin appears in the FDA import alerts SupplierRadar checked on October 26, 2026. Country-wide alerts may still apply to its products; see the Thailand page.
Has FDA refused shipments from Asisa Trakulwatt Anasin?
Yes. FDA refused 8 shipment lines from Asisa Trakulwatt Anasin between February 27, 2018 and January 21, 2020. The most recent, on January 21, 2020, was betel nut (herbal and botanicals, not teas ii), charged as POISONOUS (poisonous or deleterious substance).
Why did FDA refuse Asisa Trakulwatt Anasin's shipments?
The most frequent charges are LABELING (fair packaging and labeling act, 6 lines) and FILTHY (filthy, putrid or decomposed substance, 3 lines).
What is Asisa Trakulwatt Anasin's FEI number?
Asisa Trakulwatt Anasin's FDA Establishment Identifier (FEI) is 3013253409.

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Example subjectAsisa Trakulwatt Anasi 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.