Unimer Etamar (Plant #2)
⚠️ Moderate Risk
FEI: 3002615779 • Safi • MOROCCO
FEI Number
3002615779
Location
Safi
Country
MOROCCOAddress
220 Route Du Djorf El Youdi, , Safi, , Morocco
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
MFRHACCP
The article is subject to refusal of admission pursuant to Section 801(a)(3) of the Act in that it appears to have been prepared, packed or held under insanitary conditions whereby it may have been rendered injurious to health in that it appears to have been processed in violation of 21 CFR 123.6(a) and 123.8(a).
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 |
|---|---|---|---|
| 10/13/2016 | 16AEE33SARDINES (BRISLING, SPRATS, PILCHARDS, ETC.) | 2360HISTAMINE | Division of Northern Border Imports (DNBI) |
| 1/12/2004 | 16AEE33SARDINES (BRISLING, SPRATS, PILCHARDS, ETC.) | 2580MFRHACCP | New York District Office (NYK-DO) |
| 1/12/2004 | 16AEE33SARDINES (BRISLING, SPRATS, PILCHARDS, ETC.) | 2580MFRHACCP | New York District Office (NYK-DO) |
Frequently Asked Questions
What is Unimer Etamar (Plant #2)'s FDA import refusal history?
Unimer Etamar (Plant #2) (FEI: 3002615779) has 3 FDA import refusal record(s) in our database, spanning from 1/12/2004 to 10/13/2016.
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. Unimer Etamar (Plant #2)'s FEI number is 3002615779.
What types of violations has Unimer Etamar (Plant #2) received?
Unimer Etamar (Plant #2) has been cited for 2 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 Unimer Etamar (Plant #2) come from?
All FDA import refusal data for Unimer Etamar (Plant #2) 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.