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GRUPO VITAL

⚠️ Moderate Risk

FEI: 3013203829 • Tehuacan, Puebla • MEXICO

FEI

FEI Number

3013203829

📍

Location

Tehuacan, Puebla

🇲🇽

Country

MEXICO
🏢

Address

Calle Bugambilia No 20 mZ 32, CP 56224, Tehuacan, Puebla, Mexico

Moderate Risk

FDA Import Risk Assessment

38.1
LowModerateHighCritical

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

Statistics

4
Total Refusals
4
Unique Violations
1/19/2023
Latest Refusal
7/28/2021
Earliest Refusal

Score Breakdown

Violation Severity
56.4×40%
Refusal Volume
25.9×30%
Recency
25.6×20%
Frequency
27.0×10%
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.

1181×

NOT LISTED

It appears the drug or device is not included in a list required by Section 510(j), or a notice or other information respecting it was not provided as required by section 510(j) or 510(k).

Refusal History

DateProductViolationsDivision
1/19/2023
41GCT99MEDICAL FOODS, N.E.C.
324NO ENGLISH
482NUTRIT LBL
75UNAPPROVED
Division of Southwest Imports (DSWI)
1/19/2023
41GCT99MEDICAL FOODS, N.E.C.
324NO ENGLISH
482NUTRIT LBL
75UNAPPROVED
Division of Southwest Imports (DSWI)
1/19/2023
54YCL99VITAMIN, MINERAL, PROTEINS AND UNCONVENTIONAL DIETARY SPECIALITIES FOR HUMANS AND ANIMALS, N.E.C.
324NO ENGLISH
482NUTRIT LBL
75UNAPPROVED
Division of Southwest Imports (DSWI)
7/28/2021
66VIL99MISCELLANEOUS PATENT MEDICINES, ETC.
118NOT LISTED
75UNAPPROVED
Division of Southeast Imports (DSEI)

Frequently Asked Questions

What is GRUPO VITAL's FDA import refusal history?

GRUPO VITAL (FEI: 3013203829) has 4 FDA import refusal record(s) in our database, spanning from 7/28/2021 to 1/19/2023.

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. GRUPO VITAL's FEI number is 3013203829.

What types of violations has GRUPO VITAL received?

GRUPO VITAL 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 GRUPO VITAL come from?

All FDA import refusal data for GRUPO VITAL 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.