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Pharmerika de Mexico SA de CV

✅ Low Risk

FEI: 3011280678 • Jiutepec, Morelos • MEXICO

FEI

FEI Number

3011280678

📍

Location

Jiutepec, Morelos

🇲🇽

Country

MEXICO
🏢

Address

Calle Manzana 40, Col. Paraiso, Jiutepec, Jiutepec, Morelos, Mexico

Low Risk

FDA Import Risk Assessment

24.3
LowModerateHighCritical

This firm has a minimal history of FDA import refusals with low-severity violations.

Statistics

1
Total Refusals
1
Unique Violations
9/16/2016
Latest Refusal
9/16/2016
Earliest Refusal

Score Breakdown

Violation Severity
50.0×40%
Refusal Volume
11.2×30%
Recency
0.0×20%
Frequency
10.0×10%
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

2601×

FALSE

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(a)(1 ) of the FD&C Act in that the labeling is false or misleading in any particular.

Refusal History

DateProductViolationsDivision
9/16/2016
54YCF99VITAMIN, MINERAL, PROTEINS AND UNCONVENTIONAL DIETARY SPECIALITIES FOR HUMANS AND ANIMALS, N.E.C.
260FALSE
Division of Southwest Imports (DSWI)

Frequently Asked Questions

What is Pharmerika de Mexico SA de CV's FDA import refusal history?

Pharmerika de Mexico SA de CV (FEI: 3011280678) has 1 FDA import refusal record(s) in our database, spanning from 9/16/2016 to 9/16/2016.

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. Pharmerika de Mexico SA de CV's FEI number is 3011280678.

What types of violations has Pharmerika de Mexico SA de CV received?

Pharmerika de Mexico SA de CV has been cited for 1 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 Pharmerika de Mexico SA de CV come from?

All FDA import refusal data for Pharmerika de Mexico 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.