Norma Emerita Martinez
⚠️ Moderate Risk
FEI: 3005246881 • El Salvador • EL SALVADOR
FEI Number
3005246881
Location
El Salvador
Country
EL SALVADORAddress
Arcos De Santa Elena Calle #35, , El Salvador, , El Salvador
Moderate Risk
FDA Import Risk Assessment
This firm has a moderate history of FDA import refusals. Some attention may be warranted.
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
LABELING
The article appears in violation of FPLA because of its placement, form and/or contents statement.
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)).
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.
NO ENGLISH
Required label or labeling appears to not be in English in violation of 21 C.F.R. 201.15(c)(1).
Refusal History
| Date | Product | Violations | Division |
|---|---|---|---|
| 5/7/2007 | 12AGC99CHEESE (STANDARDIZED),N.E.C. | 473LABELING | Atlanta District Office (ATL-DO) |
| 5/7/2007 | 16XYY21SHRIMP AND PRAWNS, AQUACULTURE HARVESTED FISHERY/SEAFOOD PRODUCTS | 473LABELING | Atlanta District Office (ATL-DO) |
| 5/7/2007 | 16AGY48WHITE FISH (CISCOES, LAKE HERRING, CHUBS, TULLIBEES, ETC.) | 473LABELING | Atlanta District Office (ATL-DO) |
| 5/7/2007 | 61XAY99ANTI-HISTAMINIC N.E.C. | 472NO ENGLISH | Atlanta District Office (ATL-DO) |
| 5/7/2007 | 41BGE99FOODS WITH SUPPLEMENTAL NUTRIENTS ADDED, WITH OR WITHOUT ARTIFICAL SWEETNERS | 324NO ENGLISH | Atlanta District Office (ATL-DO) |
| 5/7/2007 | 53DY02PERFUMES (FRAGRANCE PREPARATIONS) | 324NO ENGLISH | Atlanta District Office (ATL-DO) |
| 5/7/2007 | 33YGY99CANDY WITHOUT CHOCOLATE N.E.C. | 249FILTHY | Atlanta District Office (ATL-DO) |
Frequently Asked Questions
What is Norma Emerita Martinez's FDA import refusal history?
Norma Emerita Martinez (FEI: 3005246881) has 7 FDA import refusal record(s) in our database, spanning from 5/7/2007 to 5/7/2007.
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. Norma Emerita Martinez's FEI number is 3005246881.
What types of violations has Norma Emerita Martinez received?
Norma Emerita Martinez 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 Norma Emerita Martinez come from?
All FDA import refusal data for Norma Emerita Martinez 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.