Bisoen Ramadhin
⚠️ Moderate Risk
FEI: 1000528776 • Paramaribo • SURINAME
FEI Number
1000528776
Location
Paramaribo
Country
SURINAMEAddress
Saron Koloniweg No 20, , Paramaribo, , Suriname
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
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.
WRONG IDEN
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 as defined in section 403(b) of the FD&C Act. The article appears to be offered for sale under the name of another food.
MFR INSAN
The article is subject to refusal of admission pursuant to section 801(a)(1) in that the article appears to have been manufactured, processed, or packed under insanitary conditions.
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)).
Refusal History
| Date | Product | Violations | Division |
|---|---|---|---|
| 7/31/2007 | 16AGD47WEAKFISH (SEA TROUT) | 249FILTHY | Philadelphia District Office (PHI-DO) |
| 6/27/2007 | 16AJD47WEAKFISH (SEA TROUT) | 249FILTHY | Philadelphia District Office (PHI-DO) |
| 6/27/2007 | 16AJD47WEAKFISH (SEA TROUT) | 249FILTHY | Philadelphia District Office (PHI-DO) |
| 1/6/2006 | 16AJH49WHITING (KING, NORTHERN AND SILVER) | New York District Office (NYK-DO) | |
| 9/22/2003 | 16AJH37SNAPPER (RED, GRAY, MALABAR, ETC.) | 308MFR INSAN | New York District Office (NYK-DO) |
| 1/28/2003 | 16AHY10CATFISH, FRESHWATER (E.G. CHANNEL, BLUE, WHITE, YAQUI, BULLHEAD, FLATHEAD CATFISH) | 319WRONG IDEN | New York District Office (NYK-DO) |
Frequently Asked Questions
What is Bisoen Ramadhin's FDA import refusal history?
Bisoen Ramadhin (FEI: 1000528776) has 6 FDA import refusal record(s) in our database, spanning from 1/28/2003 to 7/31/2007.
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. Bisoen Ramadhin's FEI number is 1000528776.
What types of violations has Bisoen Ramadhin received?
Bisoen Ramadhin 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 Bisoen Ramadhin come from?
All FDA import refusal data for Bisoen Ramadhin 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.