Broncolin, S.A. de C.V.
⚠️ High Risk
FEI: 3009331372 • Ciudad De Mexico, Ciudad de Mexico • MEXICO
FEI Number
3009331372
Location
Ciudad De Mexico, Ciudad de Mexico
Country
MEXICOAddress
Calle Sur 16 No. 353, Col. Agricola Oriental, Iztacalco, Ciudad De Mexico, Ciudad de Mexico, Mexico
High Risk
FDA Import Risk Assessment
This firm has a significant history of FDA import refusals with notable violations.
Statistics
Score Breakdown
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
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).
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).
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)).
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.
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.
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.
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.
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.
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
| Date | Product | Violations | Division |
|---|---|---|---|
| 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) | 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) | 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) | Division of Southwest Imports (DSWI) | |
| 3/17/2021 | 62HAY05ETHYL ALCOHOL (ANTI-MICROBIAL) | 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. | Southwest Import District Office (SWI-DO) | |
| 2/26/2015 | 54EYT99HERBALS & BOTANICAL TEAS, N.E.C. | Southwest Import District Office (SWI-DO) | |
| 7/17/2014 | 33LGY02CARAMEL CANDY PIECES, SOFT, WITHOUT NUTS AND FRUIT (WITHOUT CHOCOLATE) | 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.