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PT Heinz ABC Indonesia

⚠️ Moderate Risk

FEI: 3004352742 • Jakarta, Jakarta Raya • INDONESIA

FEI

FEI Number

3004352742

📍

Location

Jakarta, Jakarta Raya

🇮🇩

Country

INDONESIA
🏢

Address

Jl. Peta Selatan No. 48a Kalideres, , Jakarta, Jakarta Raya, Indonesia

Moderate Risk

FDA Import Risk Assessment

48.4
LowModerateHighCritical

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

Statistics

10
Total Refusals
4
Unique Violations
8/8/2007
Latest Refusal
1/21/2002
Earliest Refusal

Score Breakdown

Violation Severity
87.5×40%
Refusal Volume
38.6×30%
Recency
0.0×20%
Frequency
18.0×10%
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

117×

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).

833×

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.

2491×

FILTHY

The article is subject to refusal of admission pursuant to Section 801(a)(3) in that the article appears to consist in whole or in part of a filthy, putrid, or decomposed substance or be otherwise unfit for food.

621×

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).

Refusal History

DateProductViolationsDivision
8/8/2007
36BCT99SYRUPS AND MOLASSES, N.E.C.
62NEEDS FCE
83NO PROCESS
Los Angeles District Office (LOS-DO)
8/8/2007
36BCT99SYRUPS AND MOLASSES, N.E.C.
11UNSAFE COL
Los Angeles District Office (LOS-DO)
8/8/2007
36BCT99SYRUPS AND MOLASSES, N.E.C.
11UNSAFE COL
Los Angeles District Office (LOS-DO)
5/3/2005
36BCT99SYRUPS AND MOLASSES, N.E.C.
11UNSAFE COL
Los Angeles District Office (LOS-DO)
5/3/2005
36BCT99SYRUPS AND MOLASSES, N.E.C.
11UNSAFE COL
Los Angeles District Office (LOS-DO)
9/3/2004
36BCT99SYRUPS AND MOLASSES, N.E.C.
11UNSAFE COL
Los Angeles District Office (LOS-DO)
9/3/2004
36BCT99SYRUPS AND MOLASSES, N.E.C.
11UNSAFE COL
Los Angeles District Office (LOS-DO)
12/18/2003
36BCT99SYRUPS AND MOLASSES, N.E.C.
11UNSAFE COL
Los Angeles District Office (LOS-DO)
1/21/2002
30BEE06BEVERAGE BASE, SUBTROPICAL OR TROPICAL FRUIT, LIQUID
249FILTHY
83NO PROCESS
Los Angeles District Office (LOS-DO)
1/21/2002
30BEE99FRUIT BEVERAGE BASES, LIQUID, N.E.C.
83NO PROCESS
Los Angeles District Office (LOS-DO)

Frequently Asked Questions

What is PT Heinz ABC Indonesia's FDA import refusal history?

PT Heinz ABC Indonesia (FEI: 3004352742) has 10 FDA import refusal record(s) in our database, spanning from 1/21/2002 to 8/8/2007.

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. PT Heinz ABC Indonesia's FEI number is 3004352742.

What types of violations has PT Heinz ABC Indonesia received?

PT Heinz ABC Indonesia 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 PT Heinz ABC Indonesia come from?

All FDA import refusal data for PT Heinz ABC Indonesia 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.