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Dulceria Los Alamos S.A. De C.V.

⚠️ Moderate Risk

FEI: 3009759536 • Santiago, Nl • MEXICO

FEI

FEI Number

3009759536

📍

Location

Santiago, Nl

🇲🇽

Country

MEXICO
🏢

Address

Central # 303, , Santiago, Nl, Mexico

Moderate Risk

FDA Import Risk Assessment

41.0
LowModerateHighCritical

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

Statistics

5
Total Refusals
3
Unique Violations
5/28/2019
Latest Refusal
5/25/2016
Earliest Refusal

Score Breakdown

Violation Severity
76.7×40%
Refusal Volume
28.8×30%
Recency
0.0×20%
Frequency
16.6×10%
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

3083×

MFR INSAN

The article is subject to refusal of admission pursuant to section 801(a)(1) in that the article appears to have been manufactured, processed, or packed under insanitary conditions.

28602×

VETDRUGRES

The article is subject to refusal of admission pursuant to Section 801(a)(3) in that it appears to contain a new animal drug (or conversion product thereof) that is unsafe within the meaning of Section 512. Product contains

2561×

INCONSPICU

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
5/28/2019
16JGH05SHRIMP & PRAWNS
2860VETDRUGRES
Division of Southwest Imports (DSWI)
11/6/2018
16JGH05SHRIMP & PRAWNS
256INCONSPICU
2860VETDRUGRES
Division of Southwest Imports (DSWI)
8/25/2016
16AGH99FISH, N.E.C.
308MFR INSAN
Southwest Import District Office (SWI-DO)
5/25/2016
16AGH99FISH, N.E.C.
308MFR INSAN
Southwest Import District Office (SWI-DO)
5/25/2016
16AGH99FISH, N.E.C.
308MFR INSAN
Southwest Import District Office (SWI-DO)

Frequently Asked Questions

What is Dulceria Los Alamos S.A. De C.V.'s FDA import refusal history?

Dulceria Los Alamos S.A. De C.V. (FEI: 3009759536) has 5 FDA import refusal record(s) in our database, spanning from 5/25/2016 to 5/28/2019.

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. Dulceria Los Alamos S.A. De C.V.'s FEI number is 3009759536.

What types of violations has Dulceria Los Alamos S.A. De C.V. received?

Dulceria Los Alamos S.A. De C.V. has been cited for 3 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 Dulceria Los Alamos S.A. De C.V. come from?

All FDA import refusal data for Dulceria Los Alamos S.A. De C.V. 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.