Cepromar S.A.
⚠️ High Risk
FEI: 3004899378 • Guayaquil, Guayas • ECUADOR
FEI Number
3004899378
Location
Guayaquil, Guayas
Country
ECUADORAddress
Los Ranchos sl.15 mz 84 via a Daule, Km 12, Guayaquil, Guayas, Ecuador
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
FILTHY
The article is subject to refusal of admission pursuant to Section 801(a)(3) in that the article appears to consist in whole or in part of a filthy, putrid, or decomposed substance or be otherwise unfit for food.
POISONOUS
The article is subject to refusal of admission pursuant to Section 801(a)(3) in that it appears to bear or contain a poisonous or deleterious substance which may render the article injurious to health. Contains:
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)).
HISTAMINE
The article appears to bear or contain histamine, a poisonous and deleterious substance in such quantity as ordinarily renders it injurious to health.
Refusal History
| Date | Product | Violations | Division |
|---|---|---|---|
| 8/14/2023 | 16AYD49WHITING (KING, NORTHERN AND SILVER) | 249FILTHY | Division of Northeast Imports (DNEI) |
| 12/22/2016 | 16AGT51MAHI MAHI | Florida District Office (FLA-DO) | |
| 6/15/2016 | 16AGT51MAHI MAHI | 249FILTHY | Florida District Office (FLA-DO) |
| 7/11/2012 | 16AGT42SWORDFISH | 251POISONOUS | Florida District Office (FLA-DO) |
| 7/2/2012 | 16AGD42SWORDFISH | 251POISONOUS | Florida District Office (FLA-DO) |
| 6/14/2012 | 16AGT42SWORDFISH | 251POISONOUS | Florida District Office (FLA-DO) |
| 10/14/2010 | 16JGT05SHRIMP & PRAWNS | Los Angeles District Office (LOS-DO) | |
| 10/14/2010 | 16JGT05SHRIMP & PRAWNS | Los Angeles District Office (LOS-DO) | |
| 2/18/2009 | 16AAD51MAHI MAHI | 249FILTHY | Los Angeles District Office (LOS-DO) |
Frequently Asked Questions
What is Cepromar S.A.'s FDA import refusal history?
Cepromar S.A. (FEI: 3004899378) has 9 FDA import refusal record(s) in our database, spanning from 2/18/2009 to 8/14/2023.
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. Cepromar S.A.'s FEI number is 3004899378.
What types of violations has Cepromar S.A. received?
Cepromar 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 Cepromar S.A. come from?
All FDA import refusal data for Cepromar 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.