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Kf Udarnitca

FDA import alert and refusal historyMoscow, RussiaFEI 3015132893

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

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As of October 26, 2026, Kf Udarnitca is not on any FDA import alert in SupplierRadar's records; FDA refused 1 of its shipment line on June 30, 2022, most often for color additive unsafe under section 721 (UNSAFE COL).

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

Current status

Import alerts
Not listed
Last import refusal
Apple, jam, jelly, preserves, marmalade, butter and candied · UNSAFE COL
Last warning letter
None found
Last inspection
None on record

Every FDA record for Kf Udarnitca

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

2022

  1. Import refusal
    Refused, Apple, jam, jelly, preserves, marmalade, butter and candiedUNSAFE COLEntry BQL-0087956-7
    Source

Refusal charges, in plain English

  • UNSAFE COL1 refused line

    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 Kf Udarnitca

Is Kf Udarnitca on an FDA import alert?
No listing for Kf Udarnitca appears in the FDA import alerts SupplierRadar checked on October 26, 2026. Country-wide alerts may still apply to its products; see the Russia page.
Has FDA refused shipments from Kf Udarnitca?
Yes. FDA refused 1 shipment line from Kf Udarnitca on June 30, 2022. The most recent, on June 30, 2022, was apple, jam, jelly, preserves, marmalade, butter and candied, charged as UNSAFE COL (color additive unsafe under section 721).
Why did FDA refuse Kf Udarnitca's shipments?
The most frequent charge is UNSAFE COL (color additive unsafe under section 721, 1 line).
What is Kf Udarnitca's FEI number?
Kf Udarnitca's FDA Establishment Identifier (FEI) is 3015132893.

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Example subjectKf Udarnitc 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.