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Broncolin, S.A. de C.V.

⚠️ High Risk

FEI: 3009331372 • Ciudad De Mexico, Ciudad de Mexico • MEXICO

FEI

FEI Number

3009331372

📍

Location

Ciudad De Mexico, Ciudad de Mexico

🇲🇽

Country

MEXICO
🏢

Address

Calle Sur 16 No. 353, Col. Agricola Oriental, Iztacalco, Ciudad De Mexico, Ciudad de Mexico, Mexico

High Risk

FDA Import Risk Assessment

65.5
LowModerateHighCritical

This firm has a significant history of FDA import refusals with notable violations.

Statistics

45
Total Refusals
10
Unique Violations
10/24/2024
Latest Refusal
3/30/2009
Earliest Refusal

Score Breakdown

Violation Severity
72.5×40%
Refusal Volume
61.6×30%
Recency
75.7×20%
Frequency
28.9×10%
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

2724×

DRUG GMPS

The article is subject to refusal of admission pursuant to Section 801(a)(3) in that the methods used in and controls used for the manufacture, processing, packing, or holding of drugs and other products do not appear to conform to current good manufacturing practices within the meaning of Section 501(a)(2)(B).

7513×

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).

3247×

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)).

2923×

SUBSTITUTE

It appears to be a drug that a substance has been substituted wholly or in part.

4822×

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.

1152×

DR QUALITY

The article is subject to refusal of admission pursuant to Section 801(a)(3) in that the article appears to be represented as a drug the name of which is recognized in an official compendium and its strength appears to differ from or its quality or purity appear to fall below the standards set forth in such compendium.

2181×

LIST INGRE

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(i)(2) of the FD&C Act in that it is fabricated from two or more ingredients and the label fails to bear the common or usual name of each such ingredient and/or the article purports to be a beverage containing vegetable or fruit juice, but does not bear a statement with appropriate prominence on the information panel of the total percentage of such fruit or vegetable juice contained in the food.

3311×

DR QUALITC

The article is subject to refusal of admission pursuant to Section 801(a)(3) in that the drug appears to be represented as not being recognized in an official compendium and appears its strength differs from or its quality or purity falls below, that which it purports or is represented to possess.

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.

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.

Refusal History

DateProductViolationsDivision
10/24/2024
60LDA01ACETAMINOPHEN (ANALGESIC)
75UNAPPROVED
Division of Southeast Imports (DSEI)
4/24/2024
54YGY99VITAMIN, MINERAL, PROTEINS AND UNCONVENTIONAL DIETARY SPECIALITIES FOR HUMANS AND ANIMALS, N.E.C.
75UNAPPROVED
Division of Southeast Imports (DSEI)
4/21/2023
33SGT06LOLLIPOP (WITHOUT CHOCOLATE)
324NO ENGLISH
482NUTRIT LBL
Division of Southwest Imports (DSWI)
2/1/2022
62HAY05ETHYL ALCOHOL (ANTI-MICROBIAL)
27DRUG GMPS
Division of Southwest Imports (DSWI)
2/1/2022
62HAY05ETHYL ALCOHOL (ANTI-MICROBIAL)
27DRUG GMPS
Division of Southwest Imports (DSWI)
2/1/2022
62HAY05ETHYL ALCOHOL (ANTI-MICROBIAL)
27DRUG GMPS
Division of Southwest Imports (DSWI)
10/20/2021
62HAY05ETHYL ALCOHOL (ANTI-MICROBIAL)
27DRUG GMPS
Division of Southwest Imports (DSWI)
10/20/2021
62HAY05ETHYL ALCOHOL (ANTI-MICROBIAL)
27DRUG GMPS
Division of Southwest Imports (DSWI)
4/7/2021
62HAY05ETHYL ALCOHOL (ANTI-MICROBIAL)
27DRUG GMPS
292SUBSTITUTE
75UNAPPROVED
Division of Southwest Imports (DSWI)
4/7/2021
62HAY05ETHYL ALCOHOL (ANTI-MICROBIAL)
27DRUG GMPS
Division of Southwest Imports (DSWI)
4/7/2021
62HAY05ETHYL ALCOHOL (ANTI-MICROBIAL)
27DRUG GMPS
Division of Southwest Imports (DSWI)
3/17/2021
62HAY05ETHYL ALCOHOL (ANTI-MICROBIAL)
292SUBSTITUTE
75UNAPPROVED
Division of Southwest Imports (DSWI)
3/17/2021
62HAY05ETHYL ALCOHOL (ANTI-MICROBIAL)
27DRUG GMPS
292SUBSTITUTE
75UNAPPROVED
Division of Southwest Imports (DSWI)
3/17/2021
62HAY05ETHYL ALCOHOL (ANTI-MICROBIAL)
27DRUG GMPS
Division of Southwest Imports (DSWI)
1/8/2021
62MBY08MENTHOL (ANTI-PRURITIC)
27DRUG GMPS
Division of Southwest Imports (DSWI)
1/8/2021
62MBY08MENTHOL (ANTI-PRURITIC)
27DRUG GMPS
Division of Southwest Imports (DSWI)
11/9/2020
66FBJ99SUPPRESSANT N.E.C.
27DRUG GMPS
Division of Southwest Imports (DSWI)
11/3/2020
62MBY08MENTHOL (ANTI-PRURITIC)
331DR QUALITC
Division of Southwest Imports (DSWI)
11/3/2020
62MBY08MENTHOL (ANTI-PRURITIC)
27DRUG GMPS
Division of Southwest Imports (DSWI)
11/3/2020
62MBY08MENTHOL (ANTI-PRURITIC)
27DRUG GMPS
Division of Southwest Imports (DSWI)
11/3/2020
62MBY08MENTHOL (ANTI-PRURITIC)
27DRUG GMPS
Division of Southwest Imports (DSWI)
11/2/2020
62MBY08MENTHOL (ANTI-PRURITIC)
27DRUG GMPS
Division of Southwest Imports (DSWI)
11/2/2020
62MBY08MENTHOL (ANTI-PRURITIC)
27DRUG GMPS
Division of Southwest Imports (DSWI)
11/2/2020
62MBY08MENTHOL (ANTI-PRURITIC)
27DRUG GMPS
Division of Southwest Imports (DSWI)
11/2/2020
62MBY08MENTHOL (ANTI-PRURITIC)
27DRUG GMPS
Division of Southwest Imports (DSWI)
11/2/2020
62MBY08MENTHOL (ANTI-PRURITIC)
27DRUG GMPS
Division of Southwest Imports (DSWI)
11/2/2020
62MBY08MENTHOL (ANTI-PRURITIC)
27DRUG GMPS
Division of Southwest Imports (DSWI)
9/14/2020
62HAL05ETHYL ALCOHOL (ANTI-MICROBIAL)
27DRUG GMPS
Division of Southwest Imports (DSWI)
9/14/2020
62HAY05ETHYL ALCOHOL (ANTI-MICROBIAL)
27DRUG GMPS
Division of Southwest Imports (DSWI)
9/19/2018
31PFT99TEA SUBSTITUTES, N.E.C.
75UNAPPROVED
Division of Southwest Imports (DSWI)
9/21/2017
62MBY08MENTHOL (ANTI-PRURITIC)
115DR QUALITY
Division of Southwest Imports (DSWI)
6/9/2017
62MBY08MENTHOL (ANTI-PRURITIC)
115DR QUALITY
Division of Southwest Imports (DSWI)
9/14/2015
54EYT99HERBALS & BOTANICAL TEAS, N.E.C.
324NO ENGLISH
75UNAPPROVED
Southwest Import District Office (SWI-DO)
2/26/2015
54EYT99HERBALS & BOTANICAL TEAS, N.E.C.
482NUTRIT LBL
75UNAPPROVED
Southwest Import District Office (SWI-DO)
7/17/2014
33LGY02CARAMEL CANDY PIECES, SOFT, WITHOUT NUTS AND FRUIT (WITHOUT CHOCOLATE)
218LIST INGRE
320LACKS FIRM
324NO ENGLISH
Southwest Import District Office (SWI-DO)
2/7/2012
33SGT99CANDY SPECIALTIES, N.E.C. (WITHOUT CHOCOLATE)
324NO ENGLISH
Southwest Import District Office (SWI-DO)
2/7/2012
33SGT99CANDY SPECIALTIES, N.E.C. (WITHOUT CHOCOLATE)
324NO ENGLISH
Southwest Import District Office (SWI-DO)
2/7/2012
33SGT99CANDY SPECIALTIES, N.E.C. (WITHOUT CHOCOLATE)
324NO ENGLISH
Southwest Import District Office (SWI-DO)
2/7/2012
33SGT99CANDY SPECIALTIES, N.E.C. (WITHOUT CHOCOLATE)
324NO ENGLISH
Southwest Import District Office (SWI-DO)
2/2/2012
66VRY99MISCELLANEOUS PATENT MEDICINES, ETC.
75UNAPPROVED
Southwest Import District Office (SWI-DO)
2/2/2012
66VRY99MISCELLANEOUS PATENT MEDICINES, ETC.
75UNAPPROVED
Southwest Import District Office (SWI-DO)
2/2/2012
66VBR99MISCELLANEOUS PATENT MEDICINES, ETC.
75UNAPPROVED
Southwest Import District Office (SWI-DO)
9/17/2009
41BGT99FOODS WITH SUPPLEMENTAL NUTRIENTS ADDED, WITH OR WITHOUT ARTIFICAL SWEETNERS
488HEALTH C
Southwest Import District Office (SWI-DO)
3/30/2009
62MBY08MENTHOL (ANTI-PRURITIC)
75UNAPPROVED
Southwest Import District Office (SWI-DO)
3/30/2009
62MBY08MENTHOL (ANTI-PRURITIC)
75UNAPPROVED
Southwest Import District Office (SWI-DO)

Frequently Asked Questions

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

Broncolin, S.A. de C.V. (FEI: 3009331372) has 45 FDA import refusal record(s) in our database, spanning from 3/30/2009 to 10/24/2024.

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. Broncolin, S.A. de C.V.'s FEI number is 3009331372.

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

Broncolin, S.A. de C.V. has been cited for 10 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 Broncolin, S.A. de C.V. come from?

All FDA import refusal data for Broncolin, 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.