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Pharmaroth Latin America Sa De Cv

⚠️ Moderate Risk

FEI: 3005303473 • Mexicomexico • MEXICO

FEI

FEI Number

3005303473

📍

Location

Mexicomexico

🇲🇽

Country

MEXICO
🏢

Address

Baja California # 255torre "A" Oficina, , Mexicomexico, , Mexico

Moderate Risk

FDA Import Risk Assessment

29.8
LowModerateHighCritical

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

Statistics

4
Total Refusals
2
Unique Violations
12/15/2005
Latest Refusal
11/9/2005
Earliest Refusal

Score Breakdown

Violation Severity
45.0×40%
Refusal Volume
25.9×30%
Recency
0.0×20%
Frequency
40.0×10%
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

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)).

751×

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).

Refusal History

DateProductViolationsDivision
12/15/2005
66VCA99MISCELLANEOUS PATENT MEDICINES, ETC.
75UNAPPROVED
Cincinnati District Office (CIN-DO)
11/17/2005
54FCA99HERBALS & BOTANICALS (NOT TEAS), N.E.C.
324NO ENGLISH
Cincinnati District Office (CIN-DO)
11/9/2005
54YBC99VITAMIN, MINERAL, PROTEINS AND UNCONVENTIONAL DIETARY SPECIALITIES FOR HUMANS AND ANIMALS, N.E.C.
324NO ENGLISH
Cincinnati District Office (CIN-DO)
11/9/2005
54YBC99VITAMIN, MINERAL, PROTEINS AND UNCONVENTIONAL DIETARY SPECIALITIES FOR HUMANS AND ANIMALS, N.E.C.
324NO ENGLISH
Cincinnati District Office (CIN-DO)

Frequently Asked Questions

What is Pharmaroth Latin America Sa De Cv's FDA import refusal history?

Pharmaroth Latin America Sa De Cv (FEI: 3005303473) has 4 FDA import refusal record(s) in our database, spanning from 11/9/2005 to 12/15/2005.

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. Pharmaroth Latin America Sa De Cv's FEI number is 3005303473.

What types of violations has Pharmaroth Latin America Sa De Cv received?

Pharmaroth Latin America Sa De Cv 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 Pharmaroth Latin America Sa De Cv come from?

All FDA import refusal data for Pharmaroth Latin America Sa De Cv 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.