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Ghortex

FDA import alert and refusal historyGuatemala, GuatemalaFEI 3004313547

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Example subjectGhorte added to Import Alert 16-129 (red list)

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As of October 25, 2026, Ghortex is not on any FDA import alert in SupplierRadar's records; FDA refused 2 of its shipment lines between November 30, 2016 and December 1, 2016, most often for pesticide chemical residue (PESTICIDE).

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

Current status

Import alerts
Not listed
Last import refusal
Snow peas · PESTICIDE
Last warning letter
None found
Last inspection
Classified VAI (Voluntary Action Indicated)

Every FDA record for Ghortex

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

2016

  1. Import refusal
    Refused, Snow peasPESTICIDEEntry DM4-0472748-7
    Source
  2. Import refusal
    Refused, Snow peasPESTICIDEEntry DM4-0474158-7
    Source

2015

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

Refusal charges, in plain English

  • PESTICIDE2 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.

Questions about Ghortex

Is Ghortex on an FDA import alert?
No listing for Ghortex appears in the FDA import alerts SupplierRadar checked on October 25, 2026. Country-wide alerts may still apply to its products; see the Guatemala page.
Has FDA refused shipments from Ghortex?
Yes. FDA refused 2 shipment lines from Ghortex between November 30, 2016 and December 1, 2016. The most recent, on December 1, 2016, was snow peas, charged as PESTICIDE (pesticide chemical residue).
Why did FDA refuse Ghortex's shipments?
The most frequent charge is PESTICIDE (pesticide chemical residue, 2 lines).
When was Ghortex last inspected by FDA?
FDA's most recent inspection of Ghortex with a final classification is dated February 11, 2015 and was classified VAI (Voluntary Action Indicated).
What is Ghortex's FEI number?
Ghortex's FDA Establishment Identifier (FEI) is 3004313547.

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Example subjectGhorte 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.