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Aktieselskabet Beauvais

⚠️ Moderate Risk

FEI: 3004096063 • Tastrup • DENMARK

FEI

FEI Number

3004096063

📍

Location

Tastrup

🇩🇰

Country

DENMARK
🏢

Address

Horsvinget 1 - 3, , Tastrup, , Denmark

Moderate Risk

FDA Import Risk Assessment

45.3
LowModerateHighCritical

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

Statistics

8
Total Refusals
4
Unique Violations
7/13/2010
Latest Refusal
6/24/2003
Earliest Refusal

Score Breakdown

Violation Severity
84.0×40%
Refusal Volume
35.3×30%
Recency
0.0×20%
Frequency
11.3×10%
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

835×

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.

29202×

PESTICIDES

The article is subject to refusal of admission pursuant to section 801(a)(3) in that it appears to be adulterated because it contains a pesticide chemical, which is in violation of section 402(a)(2)(B). Contains:

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).

2411×

PESTICIDE

The article is subject to refusal of admission pursuant to Section 801(a)(3) in that it appears to bear or contain a pesticide chemical residue, which causes the article to be adulterated within the meaning of section 402(a)(2)(B) of the FD&C Act. Bears or contains:

Refusal History

DateProductViolationsDivision
7/13/2010
21CCT99MIXED FRUIT, JAM, JELLY, PRESERVES, MARMALADE, BUTTER OR CANDIED, N.E.C.
2920PESTICIDES
Seattle District Office (SEA-DO)
6/1/2010
16AET21HERRING
62NEEDS FCE
83NO PROCESS
San Francisco District Office (SAN-DO)
6/1/2010
24TCP08CABBAGE (LEAF & STEM VEGETABLE)
62NEEDS FCE
83NO PROCESS
San Francisco District Office (SAN-DO)
5/19/2010
21CCT99MIXED FRUIT, JAM, JELLY, PRESERVES, MARMALADE, BUTTER OR CANDIED, N.E.C.
2920PESTICIDES
Seattle District Office (SEA-DO)
10/18/2004
25ECE99MIXED VEGETABLES, N.E.C.
83NO PROCESS
Atlanta District Office (ATL-DO)
10/18/2004
24FCE20CUCUMBERS (FRUIT USED AS VEGETABLE)
83NO PROCESS
Atlanta District Office (ATL-DO)
10/18/2004
25LCE99ROOT & TUBER VEGETABLE, DRIED OR PASTE, N.E.C.
83NO PROCESS
Atlanta District Office (ATL-DO)
6/24/2003
20CCT14STRAWBERRY, JAM, JELLY, PRESERVES, MARMALADE, BUTTER AND CANDIED
241PESTICIDE
Seattle District Office (SEA-DO)

Frequently Asked Questions

What is Aktieselskabet Beauvais's FDA import refusal history?

Aktieselskabet Beauvais (FEI: 3004096063) has 8 FDA import refusal record(s) in our database, spanning from 6/24/2003 to 7/13/2010.

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. Aktieselskabet Beauvais's FEI number is 3004096063.

What types of violations has Aktieselskabet Beauvais received?

Aktieselskabet Beauvais 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 Aktieselskabet Beauvais come from?

All FDA import refusal data for Aktieselskabet Beauvais 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.