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Arnotts Biscuits Ltd.

⚠️ Moderate Risk

FEI: 3003717343 • Davenport • NEW ZEALAND

FEI

FEI Number

3003717343

📍

Location

Davenport

🇳🇿
🏢

Address

Unknown Street, , Davenport, , New Zealand

Moderate Risk

FDA Import Risk Assessment

31.2
LowModerateHighCritical

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

Statistics

4
Total Refusals
5
Unique Violations
4/29/2003
Latest Refusal
4/29/2003
Earliest Refusal

Score Breakdown

Violation Severity
48.6×40%
Refusal Volume
25.9×30%
Recency
0.0×20%
Frequency
40.0×10%
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

113×

UNSAFE COL

The article appears to be, or to bear or contain a color additive which is unsafe within the meaning of Section 721(a).

2183×

LIST INGRE

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(i)(2) of the FD&C Act in that it is fabricated from two or more ingredients and the label fails to bear the common or usual name of each such ingredient and/or the article purports to be a beverage containing vegetable or fruit juice, but does not bear a statement with appropriate prominence on the information panel of the total percentage of such fruit or vegetable juice contained in the food.

2743×

COLOR LBLG

The article appears to contain an artificial coloring and it fails to bear labeling stating that fact.

3213×

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.

4822×

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.

Refusal History

DateProductViolationsDivision
4/29/2003
03HFT99PLAIN COOKIES,BISCUITS AND WAFERS, N.E.C.
274COLOR LBLG
321LACKS N/C
San Francisco District Office (SAN-DO)
4/29/2003
03HFT99PLAIN COOKIES,BISCUITS AND WAFERS, N.E.C.
11UNSAFE COL
218LIST INGRE
482NUTRIT LBL
San Francisco District Office (SAN-DO)
4/29/2003
03HFT99PLAIN COOKIES,BISCUITS AND WAFERS, N.E.C.
11UNSAFE COL
218LIST INGRE
274COLOR LBLG
321LACKS N/C
482NUTRIT LBL
San Francisco District Office (SAN-DO)
4/29/2003
03HFT99PLAIN COOKIES,BISCUITS AND WAFERS, N.E.C.
11UNSAFE COL
218LIST INGRE
274COLOR LBLG
321LACKS N/C
San Francisco District Office (SAN-DO)

Frequently Asked Questions

What is Arnotts Biscuits Ltd.'s FDA import refusal history?

Arnotts Biscuits Ltd. (FEI: 3003717343) has 4 FDA import refusal record(s) in our database, spanning from 4/29/2003 to 4/29/2003.

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. Arnotts Biscuits Ltd.'s FEI number is 3003717343.

What types of violations has Arnotts Biscuits Ltd. received?

Arnotts Biscuits Ltd. has been cited for 5 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 Arnotts Biscuits Ltd. come from?

All FDA import refusal data for Arnotts Biscuits Ltd. 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.