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General Industries & Packages Co.

⚠️ Moderate Risk

FEI: 3016483140 • Taiz, Taizz • YEMEN

FEI

FEI Number

3016483140

📍

Location

Taiz, Taizz

🇾🇪

Country

YEMEN
🏢

Address

# 202, Al Hoban Area, Airport Road Unit, , Taiz, Taizz, Yemen

Moderate Risk

FDA Import Risk Assessment

47.4
LowModerateHighCritical

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

Statistics

7
Total Refusals
7
Unique Violations
11/8/2023
Latest Refusal
10/13/2021
Earliest Refusal

Score Breakdown

Violation Severity
56.7×40%
Refusal Volume
33.5×30%
Recency
56.5×20%
Frequency
33.8×10%
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

116×

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).

2182×

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.

3212×

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.

38652×

COLORLABEL

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.

3281×

USUAL NAME

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)(1) of the FD&C Act in that the label fails to bear the common or usual name of the food, if any there be.

4821×

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.

2561×

INCONSPICU

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

DateProductViolationsDivision
11/8/2023
07BGT99FRIED SNACK FOODS, N.E.C.
11UNSAFE COL
3865COLORLABEL
Division of Northeast Imports (DNEI)
11/8/2023
07BGT99FRIED SNACK FOODS, N.E.C.
11UNSAFE COL
Division of Northeast Imports (DNEI)
9/7/2023
07BGT06POTATO CHIPS,FRIED
11UNSAFE COL
Division of Northeast Imports (DNEI)
9/6/2023
07BGT99FRIED SNACK FOODS, N.E.C.
11UNSAFE COL
Division of Northeast Imports (DNEI)
5/24/2023
07BGT06POTATO CHIPS,FRIED
11UNSAFE COL
Division of Northern Border Imports (DNBI)
12/23/2022
07BGT06POTATO CHIPS,FRIED
11UNSAFE COL
218LIST INGRE
321LACKS N/C
328USUAL NAME
3865COLORLABEL
Division of Northern Border Imports (DNBI)
10/13/2021
03MFT99COOKIE,BISCUIT,WAFER DOUGH, N.E.C.
218LIST INGRE
256INCONSPICU
321LACKS N/C
482NUTRIT LBL
Division of Northern Border Imports (DNBI)

Frequently Asked Questions

What is General Industries & Packages Co.'s FDA import refusal history?

General Industries & Packages Co. (FEI: 3016483140) has 7 FDA import refusal record(s) in our database, spanning from 10/13/2021 to 11/8/2023.

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. General Industries & Packages Co.'s FEI number is 3016483140.

What types of violations has General Industries & Packages Co. received?

General Industries & Packages Co. has been cited for 7 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 General Industries & Packages Co. come from?

All FDA import refusal data for General Industries & Packages Co. 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.