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Apicola de Allende, S.A. de C.V.

⚠️ Moderate Risk

FEI: 3008831556 • Allende, Nuevo Leon • MEXICO

FEI

FEI Number

3008831556

📍

Location

Allende, Nuevo Leon

🇲🇽

Country

MEXICO
🏢

Address

Lerdo De Tejada No. 202 Ote., Col. Centro Seccion, Allende, Nuevo Leon, Mexico

Moderate Risk

FDA Import Risk Assessment

36.0
LowModerateHighCritical

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

Statistics

8
Total Refusals
7
Unique Violations
2/11/2014
Latest Refusal
12/4/2006
Earliest Refusal

Score Breakdown

Violation Severity
60.7×40%
Refusal Volume
35.3×30%
Recency
0.0×20%
Frequency
11.1×10%
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

3154×

ADDED BULK

The article is subject to refusal of admission pursuant to Section 801(a)(3) in that the food appears to have a substance added to, mixed or packed with it so as to increase its bulk or weight, or reduce its quality or strength, or make it appear better or of greater value than it is.

2603×

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.

1182×

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).

3202×

LACKS FIRM

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(e)(1) of the FD&C Act in that the food is in package form and the label fails to bear the name and place of business of the manufacturer, packer, or distributor.

2651×

SUBSTITUTE

The article is subject to refusal of admission pursuant to Section 801(a)(3) in that it appears that a substance has been substituted wholly or in part for one or more of the article's ingredients.

4881×

HEALTH C

The article is subject to refusal of admission pursuant to Section 801(a)(3) in that it appears to be misbranded in that the label or labeling bears an unauthorized nutrient content/health claim.

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
2/11/2014
36CGE99HONEY, N.E.C.
118NOT LISTED
75UNAPPROVED
Southwest Import District Office (SWI-DO)
10/3/2011
36CGE99HONEY, N.E.C.
118NOT LISTED
Southwest Import District Office (SWI-DO)
2/29/2008
36CCT01COMB HONEY
260FALSE
320LACKS FIRM
Southwest Import District Office (SWI-DO)
2/29/2008
36CCT01COMB HONEY
260FALSE
320LACKS FIRM
Southwest Import District Office (SWI-DO)
3/2/2007
36CGE99HONEY, N.E.C.
315ADDED BULK
Southwest Import District Office (SWI-DO)
3/2/2007
36CGE99HONEY, N.E.C.
315ADDED BULK
Southwest Import District Office (SWI-DO)
3/2/2007
36CGE99HONEY, N.E.C.
260FALSE
315ADDED BULK
Southwest Import District Office (SWI-DO)
12/4/2006
36CGT04HONEY
265SUBSTITUTE
315ADDED BULK
488HEALTH C
Southwest Import District Office (SWI-DO)

Frequently Asked Questions

What is Apicola de Allende, S.A. de C.V.'s FDA import refusal history?

Apicola de Allende, S.A. de C.V. (FEI: 3008831556) has 8 FDA import refusal record(s) in our database, spanning from 12/4/2006 to 2/11/2014.

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. Apicola de Allende, S.A. de C.V.'s FEI number is 3008831556.

What types of violations has Apicola de Allende, S.A. de C.V. received?

Apicola de Allende, S.A. de C.V. has been cited for 7 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 Apicola de Allende, S.A. de C.V. come from?

All FDA import refusal data for Apicola de Allende, 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.