Chinfield S.A.
⚠️ High Risk
FEI: 3002735231 • Buenos Aires, AR-B • ARGENTINA
FEI Number
3002735231
Location
Buenos Aires, AR-B
Country
ARGENTINAAddress
Av. Bernardo Ader 3205, Munro, Buenos Aires, AR-B, Argentina
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
NEW VET DR
The article is subject to refusal of admission pursuant to Section 801(a)(3) of the Federal Food, Drug, and Cosmetic Act in that it appears to be a new animal drug that is unsafe within the meaning of Section 512(a) of the Federal Food, Drug, and Cosmetic Act as it is not the subject of an approved new animal drug application, conditionally approved new animal drug application, or index listing, and no investigational new animal drug exemption applies.
FRNMFGREG
The article is subject to refusal of admission pursuant to section 801(a)(3) in that it appears to be misbranded as defined in section 502(o) of the FD&C Act. It appears that it was manufactured, prepared, propagated, compounded, or processed in an establishment not duly registered under section 510 of the Act.
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).
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).
Refusal History
| Date | Product | Violations | Division |
|---|---|---|---|
| 4/30/2024 | 66BOK99STIMULANT N.E.C. | Division of Southeast Imports (DSEI) | |
| 4/30/2024 | 66BOK99STIMULANT N.E.C. | Division of Southeast Imports (DSEI) | |
| 4/30/2024 | 63EPY18ADENOSINE (CARDIAC DEPRESSANT (ANTI-ARRHYTHMIC)) | Division of Southeast Imports (DSEI) | |
| 4/30/2024 | 66BOK99STIMULANT N.E.C. | Division of Southeast Imports (DSEI) | |
| 3/4/2019 | 62GDA99ANTI-INFLAMMATORY N.E.C. | Division of Southeast Imports (DSEI) | |
| 4/17/2015 | 66BPL99STIMULANT N.E.C. | 72NEW VET DR | New Orleans District Office (NOL-DO) |
| 7/23/2012 | 68YYY99OTHER ANIMAL, N.E.C. ANIMAL DRUGS N.E.C. | 72NEW VET DR | Cincinnati District Office (CIN-DO) |
| 6/19/2012 | 64HOK02GUAIFENESIN (EXPECTORANT) | 75UNAPPROVED | New Orleans District Office (NOL-DO) |
| 6/19/2012 | 64HOK02GUAIFENESIN (EXPECTORANT) | 75UNAPPROVED | New Orleans District Office (NOL-DO) |
| 6/21/2011 | 68YDY99OTHER ANIMAL, N.E.C. ANIMAL DRUGS N.E.C. | 72NEW VET DR | Cincinnati District Office (CIN-DO) |
| 6/21/2011 | 68YDY99OTHER ANIMAL, N.E.C. ANIMAL DRUGS N.E.C. | 72NEW VET DR | Cincinnati District Office (CIN-DO) |
| 5/28/2009 | 68YCY02HORSES ANIMAL DRUGS N.E.C. | 72NEW VET DR | Cincinnati District Office (CIN-DO) |
Frequently Asked Questions
What is Chinfield S.A.'s FDA import refusal history?
Chinfield S.A. (FEI: 3002735231) has 12 FDA import refusal record(s) in our database, spanning from 5/28/2009 to 4/30/2024.
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. Chinfield S.A.'s FEI number is 3002735231.
What types of violations has Chinfield S.A. received?
Chinfield S.A. has been cited for 4 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 Chinfield S.A. come from?
All FDA import refusal data for Chinfield S.A. 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.