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Amira Enterprises

⚠️ Moderate Risk

FEI: 3005005734 • Saint-Laurent, Quebec • CANADA

FEI

FEI Number

3005005734

📍

Location

Saint-Laurent, Quebec

🇨🇦

Country

CANADA
🏢

Address

5375 Henri-Bourassa Blvd W, , Saint-Laurent, Quebec, Canada

Moderate Risk

FDA Import Risk Assessment

35.8
LowModerateHighCritical

This firm has a moderate history of FDA import refusals. Some attention may be warranted.

Statistics

7
Total Refusals
4
Unique Violations
7/6/2007
Latest Refusal
7/6/2007
Earliest Refusal

Score Breakdown

Violation Severity
46.9×40%
Refusal Volume
33.5×30%
Recency
0.0×20%
Frequency
70.0×10%
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

4827×

NUTRIT LBL

The article is subject to refusal of admission pursuant to Section 801(a)(3) in that it appears to be misbranded in that the label or labeling fails to bear the required nutrition information.

3215×

LACKS N/C

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(e)(2) of the FD&C Act in that the food is in package form and the label fails to bear an accurate statement of the quantity of the contents in terms of weight, measure, or numerical count in accordance with Section 403(e)(2) of the FD&C Act.

622×

NEEDS FCE

It appears the manufacturer is not registered as a low acid canned food or acidified food manufacturer pursuant to 21 CFR 108.25(c)(1) or 108.35(c)(1).

832×

NO PROCESS

The article is subject to refusal of admission pursuant to Section 801(a)(3) in that the manufacturer's failure to file a scheduled process demonstrates that the product is not being manufactured under the mandatory provisions of 21 CFR Part 108 and therefore appears to have been manufactured, processed, or packed, under insanitary conditions whereby it may have been rendered injurious to health.

Refusal History

DateProductViolationsDivision
7/6/2007
24AEN06GARBANZO BEAN
482NUTRIT LBL
62NEEDS FCE
83NO PROCESS
New York District Office (NYK-DO)
7/6/2007
24AEY05FAVA BEAN
482NUTRIT LBL
62NEEDS FCE
83NO PROCESS
New York District Office (NYK-DO)
7/6/2007
23BGT12WALNUTS, BLACK, ENGLISH OR PERSIAN, SHELLED
321LACKS N/C
482NUTRIT LBL
New York District Office (NYK-DO)
7/6/2007
20AGH10RAISINS (DRIED GRAPES) (BERRY)
321LACKS N/C
482NUTRIT LBL
New York District Office (NYK-DO)
7/6/2007
02DGH02RICE, PLAIN (WHITE OR POLISHED) PROCESSED (PACKAGED)
321LACKS N/C
482NUTRIT LBL
New York District Office (NYK-DO)
7/6/2007
28AGH45SPEARMINT, WHOLE (SPICE)
321LACKS N/C
482NUTRIT LBL
New York District Office (NYK-DO)
7/6/2007
31KYY99TEA, N.E.C.
321LACKS N/C
482NUTRIT LBL
New York District Office (NYK-DO)

Frequently Asked Questions

What is Amira Enterprises's FDA import refusal history?

Amira Enterprises (FEI: 3005005734) has 7 FDA import refusal record(s) in our database, spanning from 7/6/2007 to 7/6/2007.

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. Amira Enterprises's FEI number is 3005005734.

What types of violations has Amira Enterprises received?

Amira Enterprises 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 Amira Enterprises come from?

All FDA import refusal data for Amira Enterprises 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.