ImportRefusal LogoImportRefusal

PT. Alam Jaya

⚠️ High Risk

FEI: 3013096766 • Surabaya, Jawa Timur • INDONESIA

FEI

FEI Number

3013096766

📍

Location

Surabaya, Jawa Timur

🇮🇩

Country

INDONESIA
🏢

Address

Jln. Rungkut Industri Ii No. 25, , Surabaya, Jawa Timur, Indonesia

High Risk

FDA Import Risk Assessment

51.1
LowModerateHighCritical

This firm has a significant history of FDA import refusals with notable violations.

Statistics

10
Total Refusals
4
Unique Violations
1/31/2024
Latest Refusal
6/1/2011
Earliest Refusal

Score Breakdown

Violation Severity
66.4×40%
Refusal Volume
38.6×30%
Recency
61.1×20%
Frequency
7.9×10%
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

2495×

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.

2605×

FALSE

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(a)(1 ) of the FD&C Act in that the labeling is false or misleading in any particular.

3192×

WRONG IDEN

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 as defined in section 403(b) of the FD&C Act. The article appears to be offered for sale under the name of another food.

3282×

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.

Refusal History

DateProductViolationsDivision
1/31/2024
16AVT17GROUPERS
249FILTHY
Division of West Coast Imports (DWCI)
1/31/2024
16AVT17GROUPERS
249FILTHY
Division of West Coast Imports (DWCI)
1/31/2024
16AVT17GROUPERS
249FILTHY
Division of West Coast Imports (DWCI)
5/15/2023
16AGT37SNAPPER (RED, GRAY, MALABAR, ETC.)
260FALSE
319WRONG IDEN
328USUAL NAME
Division of West Coast Imports (DWCI)
5/3/2023
16AVT37SNAPPER (RED, GRAY, MALABAR, ETC.)
260FALSE
319WRONG IDEN
328USUAL NAME
Division of West Coast Imports (DWCI)
11/30/2018
16AVT37SNAPPER (RED, GRAY, MALABAR, ETC.)
260FALSE
Division of Southeast Imports (DSEI)
11/30/2018
16AVT37SNAPPER (RED, GRAY, MALABAR, ETC.)
260FALSE
Division of Southeast Imports (DSEI)
11/30/2018
16AVT37SNAPPER (RED, GRAY, MALABAR, ETC.)
260FALSE
Division of Southeast Imports (DSEI)
1/6/2012
16AVD37SNAPPER (RED, GRAY, MALABAR, ETC.)
249FILTHY
Florida District Office (FLA-DO)
6/1/2011
16AGT37SNAPPER (RED, GRAY, MALABAR, ETC.)
249FILTHY
Los Angeles District Office (LOS-DO)

Frequently Asked Questions

What is PT. Alam Jaya's FDA import refusal history?

PT. Alam Jaya (FEI: 3013096766) has 10 FDA import refusal record(s) in our database, spanning from 6/1/2011 to 1/31/2024.

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. Alam Jaya's FEI number is 3013096766.

What types of violations has PT. Alam Jaya received?

PT. Alam Jaya 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. Alam Jaya come from?

All FDA import refusal data for PT. Alam Jaya 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.