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PRODUCTOS FARMAC UTICOS, S.A. DEC.

⚠️ Moderate Risk

FEI: 3038296046 • Zapopan, Jalisco • MEXICO

FEI

FEI Number

3038296046

📍

Location

Zapopan, Jalisco

🇲🇽

Country

MEXICO
🏢

Address

Ave L Pez Mateos #1938con Agua Blanca Industrial, Rancheria Agua Blanca Poblado, Zapopan, Zapopan, Jalisco, Mexico

Moderate Risk

FDA Import Risk Assessment

43.2
LowModerateHighCritical

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

Statistics

1
Total Refusals
5
Unique Violations
7/21/2025
Latest Refusal
7/21/2025
Earliest Refusal

Score Breakdown

Violation Severity
52.0×40%
Refusal Volume
11.2×30%
Recency
90.3×20%
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

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).

32801×

FRNMFGREG

The article is subject to refusal of admission pursuant to section 801(a)(3) in that it appears to be misbranded as defined in section 502(o) of the FD&C Act. It appears that it was manufactured, prepared, propagated, compounded, or processed in an establishment not duly registered under section 510 of the Act.

3361×

INCONSPICU

Information required by the Act to be on the label or labeling does not appear to be conspicuous enough as to render it likely to be read and understood by the ordinary individual under customary conditions of purchase and use.

4721×

NO ENGLISH

Required label or labeling appears to not be in English in violation of 21 C.F.R. 201.15(c)(1).

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
7/21/2025
56DDY20GENTAMICIN (AMINOGLYCOSIDES)
118NOT LISTED
3280FRNMFGREG
336INCONSPICU
472NO ENGLISH
75UNAPPROVED
Division of Southeast Imports (DSEI)

Frequently Asked Questions

What is PRODUCTOS FARMAC UTICOS, S.A. DEC.'s FDA import refusal history?

PRODUCTOS FARMAC UTICOS, S.A. DEC. (FEI: 3038296046) has 1 FDA import refusal record(s) in our database, spanning from 7/21/2025 to 7/21/2025.

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. PRODUCTOS FARMAC UTICOS, S.A. DEC.'s FEI number is 3038296046.

What types of violations has PRODUCTOS FARMAC UTICOS, S.A. DEC. received?

PRODUCTOS FARMAC UTICOS, S.A. DEC. has been cited for 5 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 PRODUCTOS FARMAC UTICOS, S.A. DEC. come from?

All FDA import refusal data for PRODUCTOS FARMAC UTICOS, S.A. DEC. 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.