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Sangju Saenuri Gotgam

FDA import alert and refusal historySangju, South KoreaFEI 3011355728

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Example subjectSangju Saenuri Gotga added to Import Alert 16-129 (red list)

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As of October 26, 2026, Sangju Saenuri Gotgam is not on any FDA import alert in SupplierRadar's records; FDA refused 1 of its shipment line on May 29, 2020, 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
Persimmon, dried or paste · PESTICIDE
Last warning letter
None found
Last inspection
None on record

Every FDA record for Sangju Saenuri Gotgam

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

2020

  1. Import refusal
    Refused, Persimmon, dried or pastePESTICIDEEntry U47-2001783-7
    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 Sangju Saenuri Gotgam

Is Sangju Saenuri Gotgam on an FDA import alert?
No listing for Sangju Saenuri Gotgam appears in the FDA import alerts SupplierRadar checked on October 26, 2026. Country-wide alerts may still apply to its products; see the South Korea page.
Has FDA refused shipments from Sangju Saenuri Gotgam?
Yes. FDA refused 1 shipment line from Sangju Saenuri Gotgam on May 29, 2020. The most recent, on May 29, 2020, was persimmon, dried or paste, charged as PESTICIDE (pesticide chemical residue).
Why did FDA refuse Sangju Saenuri Gotgam's shipments?
The most frequent charge is PESTICIDE (pesticide chemical residue, 1 line).
What is Sangju Saenuri Gotgam's FEI number?
Sangju Saenuri Gotgam's FDA Establishment Identifier (FEI) is 3011355728.

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Example subjectSangju Saenuri Gotga 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.