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Asesoria y Desarrollo de Productos Naturales

FDA import alert and refusal historyGuadalajara, MexicoFEI 3030448977

Recorded by FDA as ASESORIA Y DESARROLLO DE PRODUCTOS NATURALES

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Example subjectAsesoria y Desarrollo de Productos Naturale added to Import Alert 16-129 (red list)

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As of October 26, 2026, Asesoria y Desarrollo de Productos Naturales (Guadalajara, Mexico) is on the red list of FDA Import Alert 54-16 (Foods/supplements with active pharmaceutical ingredient) for umary acido hialuronico; pharm necess & ctnr for drug/bio; antibiotics (human/animal); human and animal therapeutic biologic and biosimilar drugs; human and animal drugs, published by FDA on July 29, 2024, and has 1 FDA import refusal recorded since October 2016.

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

Current status

Last import refusal
Vitamin, mineral, proteins and unconventional dietary specialities for humans and animals, n.e.c. · NO ENGLISH
Last warning letter
None found
Last inspection
None on record

Every FDA record for Asesoria y Desarrollo de Productos Naturales

2 records, newest first. Each line links to the FDA page it came from.

2024

  1. Import alert listing
    Listed on Import Alert 54-16red listUMARY Acido Hialuronico; Pharm Necess & Ctnr For Drug/Bio; Antibiotics (Human/Animal); Human and Animal Therapeutic Biologic and Biosimilar Drugs; Human and Animal Drugs
    Source
  2. Import refusal
    Refused, Vitamin, mineral, proteins and unconventional dietary specialities for humans and animals, n.e.c.NO ENGLISHLABELINGNUTRIT LBLEntry 799-9905429-9
    Source

Refusal charges, in plain English

  • LABELING1 refused line

    Fair Packaging and Labeling Act

    The package appeared not to meet the Fair Packaging and Labeling Act because of the placement, form, or contents of a required label statement.

  • NO ENGLISH1 refused line

    Required label information not in English

    Information that must appear on the label appeared not to be given in English, or not to be repeated in every language used on the label.

  • NUTRIT LBL1 refused line

    Nutrition information missing from label

    The label or labeling appeared not to carry the nutrition information that U.S. law requires for the food.

Questions about Asesoria y Desarrollo de Productos Naturales

Is Asesoria y Desarrollo de Productos Naturales on an FDA import alert?
Yes. As of October 26, 2026, Asesoria y Desarrollo de Productos Naturales is on the red list of FDA Import Alert 54-16, “Foods/supplements with active pharmaceutical ingredient”, for umary acido hialuronico; pharm necess & ctnr for drug/bio; antibiotics (human/animal); human and animal therapeutic biologic and biosimilar drugs; human and animal drugs; FDA published the listing on July 29, 2024.
Has FDA refused shipments from Asesoria y Desarrollo de Productos Naturales?
Yes. FDA refused 1 shipment line from Asesoria y Desarrollo de Productos Naturales on April 21, 2024. The most recent, on April 21, 2024, was vitamin, mineral, proteins and unconventional dietary specialities for humans and animals, n.e.c., charged as NO ENGLISH (required label information not in english).
Why did FDA refuse Asesoria y Desarrollo de Productos Naturales's shipments?
The most frequent charges are LABELING (fair packaging and labeling act, 1 line) and NO ENGLISH (required label information not in english, 1 line).
What is Asesoria y Desarrollo de Productos Naturales's FEI number?
Asesoria y Desarrollo de Productos Naturales's FDA Establishment Identifier (FEI) is 3030448977.
Can shipments from Asesoria y Desarrollo de Productos Naturales still enter the U.S.?
Shipments of umary acido hialuronico; pharm necess & ctnr for drug/bio; antibiotics (human/animal); human and animal therapeutic biologic and biosimilar drugs; human and animal drugs from Asesoria y Desarrollo de Productos Naturales can be detained without physical examination under Import Alert 54-16; 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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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.