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Kaiming Agro Processing, Pte. Ltd. (Kava Site)

FDA import alert and refusal historyNavua, FijiFEI 3017049068

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Example subjectKaiming Agro Processing, Pte. Ltd. (Kava Site added to Import Alert 16-129 (red list)

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As of October 26, 2026, Kaiming Agro Processing, Pte. Ltd. (Kava Site) (Navua, Fiji) is on the red list of FDA Import Alert 99-19 (Food products: Salmonella) for kava, published by FDA on July 23, 2025, and has 4 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) · MFR INSAN
Last warning letter
None found
Last inspection
Classified VAI (Voluntary Action Indicated)

Every FDA record for Kaiming Agro Processing, Pte. Ltd. (Kava Site)

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

2025

  1. Import refusal
    Refused, Kava kava (herbal & botanicals, not teas)MFR INSANEntry AEK-6941307-6
    Source
  2. Import alert listing
    Listed on Import Alert 99-19red listKava
    Source
  3. Import refusal
    Refused, 2 lines in one entry: Kava kava (herbal & botanicals, not teas)MFR INSANEntry AEK-6826270-6Show 2 lines
    • Refused, Kava kava (herbal & botanicals, not teas)MFR INSANEntry AEK-6826270-6Source
    • Refused, Kava kava (herbal & botanicals, not teas)MFR INSANEntry AEK-6826270-6Source
    Source
  4. Import refusal
    Refused, Kava kava (herbal & botanicals, not teas)MFR INSANMFR INJEntry AEK-6618338-3
    Source

2022

  1. Inspection
    Inspection classified VAI (Voluntary Action Indicated)Foodborne Biological Hazards
    Source

Refusal charges, in plain English

  • MFR INSAN4 refused lines

    Insanitary manufacturing, processing or packing

    The product appeared to have been manufactured, processed, or packed under insanitary conditions, which is a ground for refusal under section 801(a)(1) of the FD&C Act.

  • MFR INJ1 refused line

    Insanitary conditions, may be injurious

    The product appeared to have been prepared, packed, or held under insanitary conditions whereby it may have been rendered injurious to health.

Questions about Kaiming Agro Processing, Pte. Ltd. (Kava Site)

Is Kaiming Agro Processing, Pte. Ltd. (Kava Site) on an FDA import alert?
Yes. As of October 26, 2026, Kaiming Agro Processing, Pte. Ltd. (Kava Site) is on the red list of FDA Import Alert 99-19, “Food products: Salmonella”, for kava; FDA published the listing on July 23, 2025.
Has FDA refused shipments from Kaiming Agro Processing, Pte. Ltd. (Kava Site)?
Yes. FDA refused 4 shipment lines from Kaiming Agro Processing, Pte. Ltd. (Kava Site) between May 1, 2025 and August 26, 2025. The most recent, on August 26, 2025, was kava kava (herbal & botanicals, not teas), charged as MFR INSAN (insanitary manufacturing, processing or packing).
Why did FDA refuse Kaiming Agro Processing, Pte. Ltd. (Kava Site)'s shipments?
The most frequent charges are MFR INSAN (insanitary manufacturing, processing or packing, 4 lines) and MFR INJ (insanitary conditions, may be injurious, 1 line).
When was Kaiming Agro Processing, Pte. Ltd. (Kava Site) last inspected by FDA?
FDA's most recent inspection of Kaiming Agro Processing, Pte. Ltd. (Kava Site) with a final classification is dated March 16, 2022 and was classified VAI (Voluntary Action Indicated).
What is Kaiming Agro Processing, Pte. Ltd. (Kava Site)'s FEI number?
Kaiming Agro Processing, Pte. Ltd. (Kava Site)'s FDA Establishment Identifier (FEI) is 3017049068.
Can shipments from Kaiming Agro Processing, Pte. Ltd. (Kava Site) still enter the U.S.?
Shipments of kava from Kaiming Agro Processing, Pte. Ltd. (Kava Site) can be detained without physical examination under Import Alert 99-19; 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 subjectKaiming Agro Processing, Pte. Ltd. (Kava Site 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.