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Gandufresh S.A.C

FDA import alert and refusal historyLima, PeruFEI 3014114227

Recorded by FDA as GANDUFRESH S.A.C

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Example subjectGandufresh S.A. added to Import Alert 16-129 (red list)

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As of October 26, 2026, Gandufresh S.A.C is not on any FDA import alert in SupplierRadar's records; FDA refused 1 of its shipment line on November 7, 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
Quinoa seed (edible seed) · PESTICIDE
Last warning letter
None found
Last inspection
None on record

Every FDA record for Gandufresh S.A.C

1 record, newest first. Each line links to the FDA page it came from.

2016

  1. Import refusal
    Refused, Quinoa seed (edible seed)PESTICIDEEntry M85-0071147-7
    Source

Refusal charges, in plain English

  • PESTICIDE1 refused line

    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 Gandufresh S.A.C

Is Gandufresh S.A.C on an FDA import alert?
No listing for Gandufresh S.A.C appears in the FDA import alerts SupplierRadar checked on October 26, 2026. Country-wide alerts may still apply to its products; see the Peru page.
Has FDA refused shipments from Gandufresh S.A.C?
Yes. FDA refused 1 shipment line from Gandufresh S.A.C on November 7, 2016. The most recent, on November 7, 2016, was quinoa seed (edible seed), charged as PESTICIDE (pesticide chemical residue).
Why did FDA refuse Gandufresh S.A.C's shipments?
The most frequent charge is PESTICIDE (pesticide chemical residue, 1 line).
What is Gandufresh S.A.C's FEI number?
Gandufresh S.A.C's FDA Establishment Identifier (FEI) is 3014114227.

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Example subjectGandufresh S.A. 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.