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G & G Food Supplies Limited

FDA import alert and refusal historyEast Grinstead, United KingdomFEI 1000468361

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As of October 26, 2026, G & G Food Supplies Limited is not on any FDA import alert in SupplierRadar's records; FDA refused 2 of its shipment lines between September 8, 2017 and January 31, 2019, most often for fair packaging and labeling act (LABELING).

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

Current status

Import alerts
Not listed
Last import refusal
Vitamin, mineral, proteins and unconventional dietary specialities for humans and animals, n.e.c. · LIST INGRE
Last warning letter
None found
Last inspection
Classified VAI (Voluntary Action Indicated)

Every FDA record for G & G Food Supplies Limited

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

2026

  1. Inspection
    Inspection classified VAI (Voluntary Action Indicated)Food Composition, Standards, Labeling and Econ
    Source

2019

  1. Import refusal
    Refused, Vitamin, mineral, proteins and unconventional dietary specialities for humans and animals, n.e.c.LIST INGRENCONTACTLABELINGNUTRIT LBLHEALTH CEntry SCS-3035969-0
    Source

2017

  1. Import refusal
    Refused, Multiple vitamins (mvi-12 vitamin combo) (vitamin)LACKS FIRMLABELINGEntry 8BV-0000316-3
    Source
  2. Inspection
    Inspection classified NAI (No Action Indicated)Food Composition, Standards, Labeling and Econ
    Source

Refusal charges, in plain English

  • LABELING2 refused lines

    Fair Packaging and Labeling Act

    The package appeared not to meet the Fair Packaging and Labeling Act because of the placement, form, or contents of a required label statement.

  • HEALTH C1 refused line

    Unauthorized nutrient content or health claim

    The label or labeling appeared to carry a nutrient content claim or health claim that is not authorized.

  • LACKS FIRM1 refused line

    Manufacturer name and address missing

    The packaged product's label appeared not to show the name and place of business of the manufacturer, packer, or distributor.

  • LIST INGRE1 refused line

    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).

  • NCONTACT1 refused line

    No U.S. adverse event contact on supplement label

    The dietary supplement label appeared not to show a U.S. address or phone number through which a serious adverse event can be reported.

  • NUTRIT LBL1 refused line

    Nutrition information missing from label

    The label or labeling appeared not to carry the nutrition information that U.S. law requires for the food.

Questions about G & G Food Supplies Limited

Is G & G Food Supplies Limited on an FDA import alert?
No listing for G & G Food Supplies Limited appears in the FDA import alerts SupplierRadar checked on October 26, 2026. Country-wide alerts may still apply to its products; see the United Kingdom page.
Has FDA refused shipments from G & G Food Supplies Limited?
Yes. FDA refused 2 shipment lines from G & G Food Supplies Limited between September 8, 2017 and January 31, 2019. The most recent, on January 31, 2019, was vitamin, mineral, proteins and unconventional dietary specialities for humans and animals, n.e.c., charged as LIST INGRE (ingredients not listed).
Why did FDA refuse G & G Food Supplies Limited's shipments?
The most frequent charges are LABELING (fair packaging and labeling act, 2 lines) and HEALTH C (unauthorized nutrient content or health claim, 1 line).
When was G & G Food Supplies Limited last inspected by FDA?
FDA's most recent inspection of G & G Food Supplies Limited with a final classification is dated February 13, 2026 and was classified VAI (Voluntary Action Indicated).
What is G & G Food Supplies Limited's FEI number?
G & G Food Supplies Limited's FDA Establishment Identifier (FEI) is 1000468361.

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Example subjectG & G Food Supplies Limite 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.