SupplierRadar

Guangxi Guilin Zhiren Food Indus

FDA import alert and refusal historyGuilin, ChinaFEI 3013843555

Recorded by FDA as GUANGXI GUILIN ZHIREN FOOD INDUS

Watch this supplier

Watch this supplier

Get an email when FDA publishes anything new on Guangxi Guilin Zhiren Food Indus.

Enter your work email and confirm with the link we send. Your first supplier is free, with no password and no card.

Example subjectGuangxi Guilin Zhiren Food Indu added to Import Alert 16-129 (red list)

Free for one supplier. No password, no card.

As of October 26, 2026, Guangxi Guilin Zhiren Food Indus is not on any FDA import alert in SupplierRadar's records; FDA refused 22 of its shipment lines between October 16, 2017 and October 31, 2017, most often for melamine (MELAMINE).

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

Current status

Import alerts
Not listed
Last import refusal
Plum, dried or paste · UNSAFE COL
Last warning letter
None found
Last inspection
None on record

Every FDA record for Guangxi Guilin Zhiren Food Indus

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

2017

  1. Import refusal
    Refused, 2 lines in one entry: Plum, dried or paste; Mango, dried or pasteUNSAFE COLCYCLAMATEDULCINSACCHARLBLEntry 9EH-0020555-1Show 2 lines
    Source
  2. Import refusal
    Refused, 20 lines in one entry: Plain cookies,biscuits and wafers, n.e.c.; Potato snacks (flavored or unflavored), vegetable snacks (other than pulses) baked and 3 morePESTICIDEMELAMINEUNFIT4FOODEntry 9EH-0020555-1Show 20 lines
    Source

Refusal charges, in plain English

  • MELAMINE20 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.

  • PESTICIDE20 refused lines

    Pesticide chemical residue

    The product appeared to contain a pesticide chemical residue that makes it adulterated under section 402(a)(2)(B) of the FD&C Act, for example a residue above the U.S. tolerance or one with no U.S. tolerance for that food.

  • UNFIT4FOOD20 refused lines

    Unfit for food

    The product appeared to be unfit for food.

  • CYCLAMATE2 refused lines

    CYCLAMATE

  • DULCIN2 refused lines

    DULCIN

  • SACCHARLBL2 refused lines

    SACCHARLBL

  • UNSAFE COL2 refused lines

    Color additive unsafe under section 721

    The product appeared to be, or to contain, a color additive that is unsafe within the meaning of section 721(a) of the FD&C Act, the section that governs which color additives may be used and how.

Questions about Guangxi Guilin Zhiren Food Indus

Is Guangxi Guilin Zhiren Food Indus on an FDA import alert?
No listing for Guangxi Guilin Zhiren Food Indus appears in the FDA import alerts SupplierRadar checked on October 26, 2026. Country-wide alerts may still apply to its products; see the China page.
Has FDA refused shipments from Guangxi Guilin Zhiren Food Indus?
Yes. FDA refused 22 shipment lines from Guangxi Guilin Zhiren Food Indus between October 16, 2017 and October 31, 2017. The most recent, on October 31, 2017, was plum, dried or paste, charged as UNSAFE COL (color additive unsafe under section 721).
Why did FDA refuse Guangxi Guilin Zhiren Food Indus's shipments?
The most frequent charges are MELAMINE (melamine, 20 lines) and PESTICIDE (pesticide chemical residue, 20 lines).
What is Guangxi Guilin Zhiren Food Indus's FEI number?
Guangxi Guilin Zhiren Food Indus's FDA Establishment Identifier (FEI) is 3013843555.

Buying from Guangxi Guilin Zhiren Food Indus?

Watch it and get the FDA record the day it changes. Free for one supplier.

Watch this supplier

Watch this supplier

Get an email when FDA publishes anything new on Guangxi Guilin Zhiren Food Indus.

Enter your work email and confirm with the link we send. Your first supplier is free, with no password and no card.

Example subjectGuangxi Guilin Zhiren Food Indu added to Import Alert 16-129 (red list)

Free for one supplier. No password, no card.

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.