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Unilever Limited Exports India

FDA import alert and refusal historyMumbai, IndiaFEI 3009982200

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Example subjectUnilever Limited Exports Indi added to Import Alert 16-129 (red list)

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As of October 27, 2026, Unilever Limited Exports India (Mumbai, India) is on the red list of FDA Import Alert 45-02 (Foods with illegal or undeclared colors) for kissan mango jam, published by FDA on August 20, 2020, 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 Unilever Limited Exports India

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

2020

  1. Import alert listing
    Listed on Import Alert 45-02red listKissan Mango Jam
    Source

Questions about Unilever Limited Exports India

Is Unilever Limited Exports India on an FDA import alert?
Yes. As of October 27, 2026, Unilever Limited Exports India is on the red list of FDA Import Alert 45-02, “Foods with illegal or undeclared colors”, for kissan mango jam; FDA published the listing on August 20, 2020.
Has FDA refused shipments from Unilever Limited Exports India?
No FDA import refusals for Unilever Limited Exports India appear in FDA's refusal data since October 2016, as of October 27, 2026.
What is Unilever Limited Exports India's FEI number?
Unilever Limited Exports India's FDA Establishment Identifier (FEI) is 3009982200.
Can shipments from Unilever Limited Exports India still enter the U.S.?
Shipments of kissan mango jam from Unilever Limited Exports India 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 subjectUnilever Limited Exports Indi 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.