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Dai Tien Vinh Company

FDA import alert and refusal historyVung Tau, VietnamFEI 3011289714

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Example subjectDai Tien Vinh Compan added to Import Alert 16-129 (red list)

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As of October 26, 2026, Dai Tien Vinh Company is not on any FDA import alert in SupplierRadar's records; FDA refused 3 of its shipment lines on August 8, 2024, most often for histamine (HISTAMINE).

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

Current status

Import alerts
Not listed
Last import refusal
Tuna (albacore, yellowfin, bluefin, skipjack, etc.) · HISTAMINE
Last warning letter
None found
Last inspection
Classified NAI (No Action Indicated)

Every FDA record for Dai Tien Vinh Company

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

2024

  1. Import refusal
    Refused, 3 lines in one entry: Tuna (albacore, yellowfin, bluefin, skipjack, etc.)HISTAMINEEntry E4K-0078391-5Show 3 lines
    • Refused, Tuna (albacore, yellowfin, bluefin, skipjack, etc.)HISTAMINEEntry E4K-0078391-5Source
    • Refused, Tuna (albacore, yellowfin, bluefin, skipjack, etc.)HISTAMINEEntry E4K-0078391-5Source
    • Refused, Tuna (albacore, yellowfin, bluefin, skipjack, etc.)HISTAMINEEntry E4K-0078391-5Source
    Source

2023

  1. Inspection
    Inspection classified NAI (No Action Indicated)Foodborne Biological Hazards
    Source

Refusal charges, in plain English

  • HISTAMINE3 refused lines

    Histamine

    The product appeared to contain histamine in a quantity that ordinarily makes it injurious to health.

Questions about Dai Tien Vinh Company

Is Dai Tien Vinh Company on an FDA import alert?
No listing for Dai Tien Vinh Company appears in the FDA import alerts SupplierRadar checked on October 26, 2026. Country-wide alerts may still apply to its products; see the Vietnam page.
Has FDA refused shipments from Dai Tien Vinh Company?
Yes. FDA refused 3 shipment lines from Dai Tien Vinh Company on August 8, 2024. The most recent, on August 8, 2024, was tuna (albacore, yellowfin, bluefin, skipjack, etc.), charged as HISTAMINE (histamine).
Why did FDA refuse Dai Tien Vinh Company's shipments?
The most frequent charge is HISTAMINE (histamine, 3 lines).
When was Dai Tien Vinh Company last inspected by FDA?
FDA's most recent inspection of Dai Tien Vinh Company with a final classification is dated June 20, 2023 and was classified NAI (No Action Indicated).
What is Dai Tien Vinh Company's FEI number?
Dai Tien Vinh Company's FDA Establishment Identifier (FEI) is 3011289714.

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Example subjectDai Tien Vinh Compan 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.