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Laboratorios Quimico Farmaceuticos de Honduras S.A. de C.V.

⚠️ Moderate Risk

FEI: 3004527566 • San Pedro Sula, Cortes • HONDURAS

FEI

FEI Number

3004527566

📍

Location

San Pedro Sula, Cortes

🇭🇳

Country

HONDURAS
🏢

Address

Km. 1 Carretera A Puerto Cortes, , San Pedro Sula, Cortes, Honduras

Moderate Risk

FDA Import Risk Assessment

34.6
LowModerateHighCritical

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

Statistics

10
Total Refusals
8
Unique Violations
7/11/2019
Latest Refusal
6/11/2010
Earliest Refusal

Score Breakdown

Violation Severity
54.8×40%
Refusal Volume
38.6×30%
Recency
0.0×20%
Frequency
11.0×10%
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

756×

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).

3244×

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)).

4823×

NUTRIT LBL

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 fails to bear the required nutrition information.

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).

23002×

DIETARYLBL

The article is subject to refusal of admission pursuant to Section 801(a)(3) of the FD&C Act in that it is a dietary supplement that appears to be misbranded within the meaning of Section 403(s)(2)(B) of the FD&C Act in that the label or labeling fails to identify the product by using the term "dietary supplement", which term may be modified with the name of such an ingredient.

4882×

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.

3201×

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.

38641×

NCONTACT

The article is subject to refusal of admission pursuant to Section 801(a)(3) of the FD&C Act in that it is a dietary supplement that appears to be misbranded within the meaning of Section 403(y) of the FD&C Act in that the dietary supplement label fails to bear a domestic address or phone number through which the responsible person (as described in section 761 of the FD&C Act) may receive a report of a serious adverse event with such dietary supplement.

Refusal History

DateProductViolationsDivision
7/11/2019
54ACL90MULTIPLE VITAMINS (MVI-12 VITAMIN COMBO) (VITAMIN)
324NO ENGLISH
3864NCONTACT
482NUTRIT LBL
Division of Southeast Imports (DSEI)
11/2/2015
54AEY99VITAMIN, N.E.C.
2300DIETARYLBL
482NUTRIT LBL
75UNAPPROVED
Division of Southeast Imports (DSEI)
4/10/2015
54YCL99VITAMIN, MINERAL, PROTEINS AND UNCONVENTIONAL DIETARY SPECIALITIES FOR HUMANS AND ANIMALS, N.E.C.
324NO ENGLISH
488HEALTH C
New Orleans District Office (NOL-DO)
5/1/2014
54BCK07IRON (MINERAL)
2300DIETARYLBL
320LACKS FIRM
324NO ENGLISH
482NUTRIT LBL
Division of Southeast Imports (DSEI)
9/30/2013
65CBL99NUTRIENT/TONIC N.E.C.
75UNAPPROVED
Division of Southeast Imports (DSEI)
2/14/2013
54BCK07IRON (MINERAL)
324NO ENGLISH
488HEALTH C
Division of Southeast Imports (DSEI)
7/20/2012
61XDK21DOXYLAMINE SUCCINATE (ANTI-HISTAMINIC)
118NOT LISTED
75UNAPPROVED
Division of Southeast Imports (DSEI)
7/20/2012
64HDK02GUAIFENESIN (EXPECTORANT)
118NOT LISTED
75UNAPPROVED
Division of Southeast Imports (DSEI)
6/11/2010
66YBL99EXHIBITS - OTHER DRUG RELATED ITEMS N.E.C.
75UNAPPROVED
Division of Southeast Imports (DSEI)
6/11/2010
66YBL99EXHIBITS - OTHER DRUG RELATED ITEMS N.E.C.
75UNAPPROVED
Division of Southeast Imports (DSEI)

Frequently Asked Questions

What is Laboratorios Quimico Farmaceuticos de Honduras S.A. de C.V.'s FDA import refusal history?

Laboratorios Quimico Farmaceuticos de Honduras S.A. de C.V. (FEI: 3004527566) has 10 FDA import refusal record(s) in our database, spanning from 6/11/2010 to 7/11/2019.

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. Laboratorios Quimico Farmaceuticos de Honduras S.A. de C.V.'s FEI number is 3004527566.

What types of violations has Laboratorios Quimico Farmaceuticos de Honduras S.A. de C.V. received?

Laboratorios Quimico Farmaceuticos de Honduras S.A. de C.V. has been cited for 8 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 Laboratorios Quimico Farmaceuticos de Honduras S.A. de C.V. come from?

All FDA import refusal data for Laboratorios Quimico Farmaceuticos de Honduras 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.