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LABORATORIOS NUTRIMED

⚠️ Moderate Risk

FEI: 3017549100 • Ciudad De Mexico, Ciudad de Mexico • MEXICO

FEI

FEI Number

3017549100

📍

Location

Ciudad De Mexico, Ciudad de Mexico

🇲🇽

Country

MEXICO
🏢

Address

Avenida Toltecas No 29, Barrio Santa Barbara, Iztapalapa, Ciudad De Mexico, Ciudad de Mexico, Mexico

Moderate Risk

FDA Import Risk Assessment

49.7
LowModerateHighCritical

This firm has a moderate history of FDA import refusals. Some attention may be warranted.

Statistics

4
Total Refusals
4
Unique Violations
9/23/2025
Latest Refusal
1/3/2023
Earliest Refusal

Score Breakdown

Violation Severity
54.2×40%
Refusal Volume
25.9×30%
Recency
94.0×20%
Frequency
14.7×10%
How is this score calculated?

Proprietary Algorithm

  • 40% Violation Severity — AI-assessed (1-10)
  • 30% Refusal Volume — Logarithmic scale
  • 20% Recency — Decays over 5 years
  • 10% Frequency — Refusals per year

© ImportRefusal.com Original Analysis

Violation Summary

754×

UNAPPROVED

The article is subject to refusal of admission pursuant to Section 801(a)(3) in that it appears to be a new drug within the meaning of Section 201(p) without an approved New Drug Application (NDA).

3243×

NO ENGLISH

The article is subject to refusal of admission pursuant to Section 801(a)(3) of the FD&C Act in that it appears to be misbranded within the meaning of Section 403(f) of the FD&C Act in that any word, statement, or other information required by or under the authority of the FD&C Act to appear on the label or labeling is not prominently placed thereon with such conspicuousness (as compared with other words, statements, designs, or devices, in the labeling) and in such terms as to render it likely to be read and understood by the ordinary individual under customary terms of purchase and use (for example, label contains information in two or more languages but fails to repeat all required information in both languages in accordance with 21 CFR 101.15(c)(2), or label fails to include all required information in English in accordance with 21 CFR 101.15(c)(1), except in the case of articles distributed solely in the Commonwealth of Puerto Rico or in a Territory where the predominant language is one other than English)).

4823×

NUTRIT LBL

The article is subject to refusal of admission pursuant to Section 801(a)(3) in that it appears to be misbranded in that the label or labeling fails to bear the required nutrition information.

38642×

NCONTACT

The article is subject to refusal of admission pursuant to Section 801(a)(3) of the FD&C Act in that it is a dietary supplement that appears to be misbranded within the meaning of Section 403(y) of the FD&C Act in that the dietary supplement label fails to bear a domestic address or phone number through which the responsible person (as described in section 761 of the FD&C Act) may receive a report of a serious adverse event with such dietary supplement.

Refusal History

DateProductViolationsDivision
9/23/2025
41YYT99DIETARY CONVENTIONAL FOODS, N.E.C.
324NO ENGLISH
3864NCONTACT
482NUTRIT LBL
75UNAPPROVED
Division of Southeast Imports (DSEI)
9/23/2025
41YYY99DIETARY CONVENTIONAL FOODS, N.E.C.
324NO ENGLISH
3864NCONTACT
482NUTRIT LBL
75UNAPPROVED
Division of Southeast Imports (DSEI)
1/19/2023
41GHT99MEDICAL FOODS, N.E.C.
324NO ENGLISH
482NUTRIT LBL
75UNAPPROVED
Division of Southwest Imports (DSWI)
1/3/2023
54YCC99VITAMIN, MINERAL, PROTEINS AND UNCONVENTIONAL DIETARY SPECIALITIES FOR HUMANS AND ANIMALS, N.E.C.
75UNAPPROVED
Division of Southeast Imports (DSEI)

Frequently Asked Questions

What is LABORATORIOS NUTRIMED's FDA import refusal history?

LABORATORIOS NUTRIMED (FEI: 3017549100) has 4 FDA import refusal record(s) in our database, spanning from 1/3/2023 to 9/23/2025.

What is an FEI number?

FEI stands for Firm Establishment Identifier. It's a unique number assigned by the FDA to identify establishments that manufacture, process, pack, or hold food, drugs, medical devices, or other FDA-regulated products. LABORATORIOS NUTRIMED's FEI number is 3017549100.

What types of violations has LABORATORIOS NUTRIMED received?

LABORATORIOS NUTRIMED has been cited for 4 different violation type(s). Common FDA violations include adulteration (unsafe or unsanitary products), misbranding (incorrect or misleading labels), and regulatory non-compliance.

Where does this information about LABORATORIOS NUTRIMED come from?

All FDA import refusal data for LABORATORIOS NUTRIMED is sourced from the official FDA Data Dashboard (datadashboard.fda.gov), a public government database maintained by the U.S. Food and Drug Administration.

Data sourced from the FDA Data Dashboard, a public database maintained by the U.S. Food and Drug Administration.