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Vicce Enterprise

FDA import alert and refusal historyTijuana, MexicoFEI 3010141933

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Example subjectVicce Enterpris added to Import Alert 16-129 (red list)

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As of October 25, 2026, Vicce Enterprise (Tijuana, Mexico) is on the red list of FDA Import Alert 99-39 (Imported foods that appear to be misbranded) for herbal supplement with l.carnitine and magnesium/ima capsules, published by FDA on January 21, 2015, 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 Vicce Enterprise

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

2015

  1. Import alert listing
    Listed on Import Alert 99-39red listHerbal supplement with L.Carnitine and Magnesium/IMA Capsules
    Source

Questions about Vicce Enterprise

Is Vicce Enterprise on an FDA import alert?
Yes. As of October 25, 2026, Vicce Enterprise is on the red list of FDA Import Alert 99-39, “Imported foods that appear to be misbranded”, for herbal supplement with l.carnitine and magnesium/ima capsules; FDA published the listing on January 21, 2015.
Has FDA refused shipments from Vicce Enterprise?
No FDA import refusals for Vicce Enterprise appear in FDA's refusal data since October 2016, as of October 25, 2026.
What is Vicce Enterprise's FEI number?
Vicce Enterprise's FDA Establishment Identifier (FEI) is 3010141933.
Can shipments from Vicce Enterprise still enter the U.S.?
Shipments of herbal supplement with l.carnitine and magnesium/ima capsules from Vicce Enterprise can be detained without physical examination under Import Alert 99-39; 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 subjectVicce Enterpris 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.