Especialidades Nutriton
FDA import alert and refusal historyZapopan, MexicoFEI 3030443314
Recorded by FDA as ESPECIALIDADES NUTRITON
As of October 26, 2026, Especialidades Nutriton is not on any FDA import alert in SupplierRadar's records; FDA refused 5 of its shipment lines between August 22, 2024 and May 18, 2026, most often for required label information not in english (NO ENGLISH).
Data from FDA public records, last checked . Request a correction
Current status
- Import alerts
- Not listed
- Last import refusal
- Vitamin, mineral, proteins and unconventional dietary specialities for humans and animals, n.e.c. · UNAPPROVED
- Last warning letter
- None found
- Last inspection
- None on record
Every FDA record for Especialidades Nutriton
5 records, newest first. Each line links to the FDA page it came from.
2026
- Import refusalRefused, Vitamin, mineral, proteins and unconventional dietary specialities for humans and animals, n.e.c.UNAPPROVEDEntry AEK-7854117-2Source
2025
- Import refusalRefused, Vitamin e (tocopherol)LIST INGREINCONSPICULACKS FIRMNO ENGLISHNCONTACTNUTRIT LBLEntry AEK-5012145-6Source
- Import refusalRefused, Vitamin e (tocopherol)LIST INGREINCONSPICULACKS FIRMNO ENGLISHNCONTACTNUTRIT LBLEntry AEK-5012142-3Source
2024
- Import refusalRefused, Vitamin, mineral, proteins and unconventional dietary specialities for humans and animals, n.e.c.NO ENGLISHEntry AEK-5562406-6Source
- Import refusalRefused, 54k[][]22/turmeric (herbal & botanicals, not teas ii)NO ENGLISHEntry AEK-5578388-8Source
Refusal charges, in plain English
- NO ENGLISH4 refused lines
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.
- INCONSPICU2 refused lines
Required information not conspicuous
Information required on the label appeared not to be placed prominently or conspicuously enough to be read and understood by an ordinary consumer.
- LACKS FIRM2 refused lines
Manufacturer name and address missing
The packaged product's label appeared not to show the name and place of business of the manufacturer, packer, or distributor.
- LIST INGRE2 refused lines
Ingredients not listed
The product is made from two or more ingredients and the label appeared not to list the common or usual name of each one (or, for a juice beverage, the percentage of juice).
- NCONTACT2 refused lines
No U.S. adverse event contact on supplement label
The dietary supplement label appeared not to show a U.S. address or phone number through which a serious adverse event can be reported.
- NUTRIT LBL2 refused lines
Nutrition information missing from label
The label or labeling appeared not to carry the nutrition information that U.S. law requires for the food.
- UNAPPROVED1 refused line
Unapproved new drug
The product appeared to be a new drug within the meaning of section 201(p) of the FD&C Act without an approved New Drug Application. FDA can apply this charge to a food or supplement whose labeling presents it for drug uses.
Questions about Especialidades Nutriton
- Is Especialidades Nutriton on an FDA import alert?
- No listing for Especialidades Nutriton appears in the FDA import alerts SupplierRadar checked on October 26, 2026. Country-wide alerts may still apply to its products; see the Mexico page.
- Has FDA refused shipments from Especialidades Nutriton?
- Yes. FDA refused 5 shipment lines from Especialidades Nutriton between August 22, 2024 and May 18, 2026. The most recent, on May 18, 2026, was vitamin, mineral, proteins and unconventional dietary specialities for humans and animals, n.e.c., charged as UNAPPROVED (unapproved new drug).
- Why did FDA refuse Especialidades Nutriton's shipments?
- The most frequent charges are NO ENGLISH (required label information not in english, 4 lines) and INCONSPICU (required information not conspicuous, 2 lines).
- What is Especialidades Nutriton's FEI number?
- Especialidades Nutriton's FDA Establishment Identifier (FEI) is 3030443314.
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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.