ImportRefusal LogoImportRefusal

Laboratorios Grossmann

⚠️ Moderate Risk

FEI: 3005206252 • Harrison • MEXICO

FEI

FEI Number

3005206252

📍

Location

Harrison

🇲🇽

Country

MEXICO
🏢

Address

Calz Detlalpan No.20 & 21, , Harrison, , Mexico

Moderate Risk

FDA Import Risk Assessment

35.5
LowModerateHighCritical

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

Statistics

3
Total Refusals
2
Unique Violations
10/25/2010
Latest Refusal
4/13/2007
Earliest Refusal

Score Breakdown

Violation Severity
70.0×40%
Refusal Volume
22.3×30%
Recency
0.0×20%
Frequency
8.5×10%
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

752×

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).

3241×

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)).

Refusal History

DateProductViolationsDivision
10/25/2010
54YDA99VITAMIN, MINERAL, PROTEINS AND UNCONVENTIONAL DIETARY SPECIALITIES FOR HUMANS AND ANIMALS, N.E.C.
75UNAPPROVED
New Orleans District Office (NOL-DO)
8/18/2009
60LDA17CLONIXIN (ANALGESIC)
75UNAPPROVED
New Orleans District Office (NOL-DO)
4/13/2007
54BCF01CALCIUM (MINERAL)
324NO ENGLISH
New Orleans District Office (NOL-DO)

Frequently Asked Questions

What is Laboratorios Grossmann's FDA import refusal history?

Laboratorios Grossmann (FEI: 3005206252) has 3 FDA import refusal record(s) in our database, spanning from 4/13/2007 to 10/25/2010.

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 Grossmann's FEI number is 3005206252.

What types of violations has Laboratorios Grossmann received?

Laboratorios Grossmann has been cited for 2 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 Grossmann come from?

All FDA import refusal data for Laboratorios Grossmann 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.