SupplierRadar

VASIFOOD TRADING PRODUCTION Co.,LTD

FDA import alert and refusal historyDuc Hoa District, VietnamFEI 3013291718

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Example subjectVASIFOOD TRADING PRODUCTION Co.,LT added to Import Alert 16-129 (red list)

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As of October 26, 2026, VASIFOOD TRADING PRODUCTION Co.,LTD is not on any FDA import alert in SupplierRadar's records; FDA refused 18 of its shipment lines between December 6, 2016 and February 10, 2026, most often for filthy, putrid or decomposed substance (FILTHY).

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

Current status

Import alerts
Not listed
Last import refusal
Tamarind, topping or syrup · FILTHY
Last warning letter
None found
Last inspection
Classified VAI (Voluntary Action Indicated)

Every FDA record for VASIFOOD TRADING PRODUCTION Co.,LTD

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

2026

  1. Import refusal
    Refused, Tamarind, topping or syrupFILTHYEntry 115-0121188-9
    Source

2024

  1. Import refusal
    Refused, Fish sauce, fishery products, n.e.c.NO PROCESSEntry U10-1233273-4
    Source

2023

  1. Import refusal
    Refused, 6 lines in one entry: Fish, n.e.c.FILTHYEntry 9T4-3037778-3Show 6 lines
    Source

2022

  1. Import refusal
    Refused, Gourmay, gouramiFILTHYEntry D52-0205795-2
    Source
  2. Import refusal
    Refused, 2 lines in one entry: Gourmay, gouramiFILTHYEntry D52-0197376-1Show 2 lines
    Source
  3. Import refusal
    Refused, 3 lines in one entry: Gourmay, gouramiFILTHYEntry 9T4-3035440-2Show 3 lines
    Source
  4. Import refusal
    Refused, 2 lines in one entry: Fish sauce, fishery products, n.e.c.FILTHYNO PROCESSEntry AVV-3020004-5Show 2 lines
    Source

2017

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

2016

  1. Import refusal
    Refused, Mackerel (only scomberomorus spp eg. spanish or king)HISTAMINEFILTHYEntry KM6-0088876-2
    Source
  2. Import refusal
    Refused, Mackerel (all except scomberomorus sp, eg spanish or king see '22')HISTAMINEFILTHYEntry J34-0079561-6
    Source

Refusal charges, in plain English

  • FILTHY17 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.

  • NO PROCESS3 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.

  • HISTAMINE2 refused lines

    Histamine

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

Questions about VASIFOOD TRADING PRODUCTION Co.,LTD

Is VASIFOOD TRADING PRODUCTION Co.,LTD on an FDA import alert?
No listing for VASIFOOD TRADING PRODUCTION 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 Vietnam page.
Has FDA refused shipments from VASIFOOD TRADING PRODUCTION Co.,LTD?
Yes. FDA refused 18 shipment lines from VASIFOOD TRADING PRODUCTION Co.,LTD between December 6, 2016 and February 10, 2026. The most recent, on February 10, 2026, was tamarind, topping or syrup, charged as FILTHY (filthy, putrid or decomposed substance).
Why did FDA refuse VASIFOOD TRADING PRODUCTION Co.,LTD's shipments?
The most frequent charges are FILTHY (filthy, putrid or decomposed substance, 17 lines) and NO PROCESS (no scheduled process filed, 3 lines).
When was VASIFOOD TRADING PRODUCTION Co.,LTD last inspected by FDA?
FDA's most recent inspection of VASIFOOD TRADING PRODUCTION Co.,LTD with a final classification is dated June 8, 2017 and was classified VAI (Voluntary Action Indicated).
What is VASIFOOD TRADING PRODUCTION Co.,LTD's FEI number?
VASIFOOD TRADING PRODUCTION Co.,LTD's FDA Establishment Identifier (FEI) is 3013291718.

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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.