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Ace Kava Exporters

FDA import alert and refusal historyNadi, FijiFEI 3011546775

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Example subjectAce Kava Exporter added to Import Alert 16-129 (red list)

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As of October 26, 2026, Ace Kava Exporters (Nadi, Fiji) is on the red list of FDA Import Alert 54-14 (Supplements from firms not meeting supplement GMP) for whole grains/milled grain products/starches; bakery products/dough/mixes/icings; macaroni/noodle products; cereal preparations/breakfast foods; snack food items; milk/butter/dried milk products; cheese/cheese products; ice cream and related products; filled milk/imitation milk products; eggs/egg pr…, published by FDA on July 17, 2020, and has 3 FDA import refusals recorded since October 2016.

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

Current status

Last import refusal
Kava kava (herbal & botanicals, not teas) · UNAPPROVED
Last warning letter
None found
Last inspection
Classified OAI (Official Action Indicated)

Every FDA record for Ace Kava Exporters

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

2021

  1. Import refusal
    Refused, Kava kava (herbal & botanicals, not teas)UNAPPROVEDEntry AEK-7731141-0
    Source

2020

  1. Import refusal
    Refused, Kava kava (herbal & botanicals, not teas)UNAPPROVEDEntry AEK-7750048-3
    Source
  2. Import alert listing
    Listed on Import Alert 54-14red listWhole Grains/Milled Grain Products/Starches; Bakery Products/Dough/Mixes/Icings; Macaroni/Noodle Products; Cereal Preparations/Breakfast Foods; Snack Food Items; Milk/Butter/Dried Milk Products; Cheese/Cheese Products; Ice Cream and related Products; Filled Milk/Imitation Milk Products; Eggs/Egg Pr…
    Source
  3. Inspection
    Inspection classified OAI (Official Action Indicated)Food Composition, Standards, Labeling and Econ
    Source

2018

  1. Import refusal
    Refused, Kava kava (herbal & botanicals, not teas)LIST INGREDIETARYLBLINCONSPICUNCONTACTEntry AEK-4197453-3
    Source

Refusal charges, in plain English

  • UNAPPROVED2 refused lines

    Unapproved new drug

    The product appeared to be a new drug within the meaning of section 201(p) of the FD&C Act without an approved New Drug Application. FDA can apply this charge to a food or supplement whose labeling presents it for drug uses.

  • DIETARYLBL1 refused line

    Not identified as a dietary supplement

    The label appeared not to identify the product with the term "dietary supplement" (which may be modified with the name of an ingredient).

  • INCONSPICU1 refused line

    Required information not conspicuous

    Information required on the label appeared not to be placed prominently or conspicuously enough to be read and understood by an ordinary consumer.

  • LIST INGRE1 refused line

    Ingredients not listed

    The product is made from two or more ingredients and the label appeared not to list the common or usual name of each one (or, for a juice beverage, the percentage of juice).

  • NCONTACT1 refused line

    No U.S. adverse event contact on supplement label

    The dietary supplement label appeared not to show a U.S. address or phone number through which a serious adverse event can be reported.

Questions about Ace Kava Exporters

Is Ace Kava Exporters on an FDA import alert?
Yes. As of October 26, 2026, Ace Kava Exporters is on the red list of FDA Import Alert 54-14, “Supplements from firms not meeting supplement GMP”, for whole grains/milled grain products/starches; bakery products/dough/mixes/icings; macaroni/noodle products; cereal preparations/breakfast foods; snack food items; milk/butter/dried milk products; cheese/cheese products; ice cream and related products; filled milk/imitation milk products; eggs/egg pr…; FDA published the listing on July 17, 2020.
Has FDA refused shipments from Ace Kava Exporters?
Yes. FDA refused 3 shipment lines from Ace Kava Exporters between February 28, 2018 and January 19, 2021. The most recent, on January 19, 2021, was kava kava (herbal & botanicals, not teas), charged as UNAPPROVED (unapproved new drug).
Why did FDA refuse Ace Kava Exporters's shipments?
The most frequent charges are UNAPPROVED (unapproved new drug, 2 lines) and DIETARYLBL (not identified as a dietary supplement, 1 line).
When was Ace Kava Exporters last inspected by FDA?
FDA's most recent inspection of Ace Kava Exporters with a final classification is dated February 26, 2020 and was classified OAI (Official Action Indicated).
What is Ace Kava Exporters's FEI number?
Ace Kava Exporters's FDA Establishment Identifier (FEI) is 3011546775.
Can shipments from Ace Kava Exporters still enter the U.S.?
Shipments of whole grains/milled grain products/starches; bakery products/dough/mixes/icings; macaroni/noodle products; cereal preparations/breakfast foods; snack food items; milk/butter/dried milk products; cheese/cheese products; ice cream and related products; filled milk/imitation milk products; eggs/egg pr… from Ace Kava Exporters can be detained without physical examination under Import Alert 54-14; 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 subjectAce Kava Exporter 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.