Quanzhou Goldenfuture Food Group CO.,LTD.
FDA import alert and refusal historyHuian, ChinaFEI 3007991582
As of October 27, 2026, Quanzhou Goldenfuture Food Group CO.,LTD. is not on any FDA import alert in SupplierRadar's records; FDA refused 6 of its shipment lines between November 15, 2016 and April 7, 2017, most often for nutrition information missing from label (NUTRIT LBL).
Data from FDA public records, last checked . Request a correction
Current status
- Import alerts
- Not listed
- Last import refusal
- Jellyfish, other aquatic species · NEEDS FCE
- Last warning letter
- None found
- Last inspection
- None on record
Every FDA record for Quanzhou Goldenfuture Food Group CO.,LTD.
6 records, newest first. Each line links to the FDA page it came from.
2017
- Import refusalRefused, Jellyfish, other aquatic speciesNEEDS FCENO PROCESSEntry KM6-3501185-1Source
- Import refusalRefused, Olives, dried or pasteCYCLAMATENUTRIT LBLEntry KM6-3500645-5Source
- Import refusalSource
Refused, 3 lines in one entry: Plain cookies,biscuits and wafers, n.e.c.; Snack foods not elsewhere mentioned, n.e.c.POISONOUSMELAMINEUNFIT4FOODLIST INGREEntry KM6-3500645-5Show 3 linesHide lines
- Refused, Plain cookies,biscuits and wafers, n.e.c.POISONOUSMELAMINEUNFIT4FOODEntry KM6-3500645-5Source
- Refused, Snack foods not elsewhere mentioned, n.e.c.LIST INGRENUTRIT LBLNO PROCESSEntry KM6-3500645-5Source
- Refused, Snack foods not elsewhere mentioned, n.e.c.LIST INGRENUTRIT LBLNO PROCESSEntry KM6-3500645-5Source
2016
- Import refusalRefused, Vegetable protein products not elsewhere mentioned, n.e.c.LIST INGREPOISONOUSUSUAL NAMEMELAMINEUNFIT4FOODNUTRIT LBLEntry KM6-0089317-6Source
Refusal charges, in plain English
- NUTRIT LBL4 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.
- LIST INGRE3 refused lines
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).
- 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.
- MELAMINE2 refused lines
Melamine
The product appeared to contain melamine or a melamine analog, which is an unsafe food additive within the meaning of section 409 of the FD&C Act.
- 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.
- UNFIT4FOOD2 refused lines
Unfit for food
The product appeared to be unfit for food.
- CYCLAMATE1 refused line
CYCLAMATE
- NEEDS FCE1 refused line
Processor not registered for canned or acidified foods
The manufacturer appeared not to be registered with FDA as a low-acid canned food or acidified food processor, as 21 CFR 108.25 and 108.35 require.
Questions about Quanzhou Goldenfuture Food Group CO.,LTD.
- Is Quanzhou Goldenfuture Food Group CO.,LTD. on an FDA import alert?
- No listing for Quanzhou Goldenfuture Food Group CO.,LTD. appears in the FDA import alerts SupplierRadar checked on October 27, 2026. Country-wide alerts may still apply to its products; see the China page.
- Has FDA refused shipments from Quanzhou Goldenfuture Food Group CO.,LTD.?
- Yes. FDA refused 6 shipment lines from Quanzhou Goldenfuture Food Group CO.,LTD. between November 15, 2016 and April 7, 2017. The most recent, on April 7, 2017, was jellyfish, other aquatic species, charged as NEEDS FCE (processor not registered for canned or acidified foods).
- Why did FDA refuse Quanzhou Goldenfuture Food Group CO.,LTD.'s shipments?
- The most frequent charges are NUTRIT LBL (nutrition information missing from label, 4 lines) and LIST INGRE (ingredients not listed, 3 lines).
- What is Quanzhou Goldenfuture Food Group CO.,LTD.'s FEI number?
- Quanzhou Goldenfuture Food Group CO.,LTD.'s FDA Establishment Identifier (FEI) is 3007991582.
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