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Lacompagnie De Kinkiliba

FDA import alert and refusal historyMarville, FranceFEI 3003994805

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Example subjectLacompagnie De Kinkilib added to Import Alert 16-129 (red list)

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As of October 26, 2026, Lacompagnie De Kinkiliba (Marville, France) is on the red list of FDA Import Alert 45-02 (Foods with illegal or undeclared colors) for rose syrup; lavender syrup; violet syrup, published by FDA on March 16, 2010, and has no FDA import refusals recorded since October 2016.

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

Current status

Last import refusal
None since October 2016
Last warning letter
None found
Last inspection
None on record

Every FDA record for Lacompagnie De Kinkiliba

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

2010

  1. Import alert listing
    Listed on Import Alert 45-02red listRose Syrup; Lavender Syrup; Violet Syrup
    Source

Questions about Lacompagnie De Kinkiliba

Is Lacompagnie De Kinkiliba on an FDA import alert?
Yes. As of October 26, 2026, Lacompagnie De Kinkiliba is on the red list of FDA Import Alert 45-02, “Foods with illegal or undeclared colors”, for rose syrup; lavender syrup; violet syrup; FDA published the listing on March 16, 2010.
Has FDA refused shipments from Lacompagnie De Kinkiliba?
No FDA import refusals for Lacompagnie De Kinkiliba appear in FDA's refusal data since October 2016, as of October 26, 2026.
What is Lacompagnie De Kinkiliba's FEI number?
Lacompagnie De Kinkiliba's FDA Establishment Identifier (FEI) is 3003994805.
Can shipments from Lacompagnie De Kinkiliba still enter the U.S.?
Shipments of rose syrup; lavender syrup; violet syrup from Lacompagnie De Kinkiliba can be detained without physical examination under Import Alert 45-02; FDA releases them only if evidence shows they do not have the listed violation. Importers must consider this listing in their FSVP evaluation (21 CFR 1.505).

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Example subjectLacompagnie De Kinkilib 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.