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PT. Marizarasa Sarimurni

⚠️ Moderate Risk

FEI: 3009797745 • Serang-Banten, Banten • INDONESIA

FEI

FEI Number

3009797745

📍

Location

Serang-Banten, Banten

🇮🇩

Country

INDONESIA
🏢

Address

Km. 8, Jl. Raya Cikande- Rangkasbitung, Serang-Banten, Banten, Indonesia

Moderate Risk

FDA Import Risk Assessment

34.0
LowModerateHighCritical

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

Statistics

4
Total Refusals
8
Unique Violations
1/25/2016
Latest Refusal
7/22/2004
Earliest Refusal

Score Breakdown

Violation Severity
64.6×40%
Refusal Volume
25.9×30%
Recency
0.0×20%
Frequency
3.5×10%
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

623×

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).

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.

2742×

COLOR LBLG

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

111×

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).

641×

YELLOW #5

The food appears to bear or contain the color additive FD & C Yellow No. 5, which is not declared on the label per 21 CFR 74.705(a)(c) under section 721.

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.

2601×

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.

4731×

LABELING

The article appears in violation of FPLA because of its placement, form and/or contents statement.

Refusal History

DateProductViolationsDivision
1/25/2016
37JHT03CHILI SAUCE
62NEEDS FCE
83NO PROCESS
Los Angeles District Office (LOS-DO)
1/25/2016
37JHT03CHILI SAUCE
62NEEDS FCE
83NO PROCESS
Los Angeles District Office (LOS-DO)
8/27/2010
23ECT05COCONUT, SPREAD
11UNSAFE COL
260FALSE
274COLOR LBLG
62NEEDS FCE
64YELLOW #5
83NO PROCESS
Los Angeles District Office (LOS-DO)
7/22/2004
03RGT01CAKE WITHOUT CUSTARD OR CREAM FILLING
274COLOR LBLG
473LABELING
482NUTRIT LBL
Los Angeles District Office (LOS-DO)

Frequently Asked Questions

What is PT. Marizarasa Sarimurni's FDA import refusal history?

PT. Marizarasa Sarimurni (FEI: 3009797745) has 4 FDA import refusal record(s) in our database, spanning from 7/22/2004 to 1/25/2016.

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. Marizarasa Sarimurni's FEI number is 3009797745.

What types of violations has PT. Marizarasa Sarimurni received?

PT. Marizarasa Sarimurni has been cited for 8 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. Marizarasa Sarimurni come from?

All FDA import refusal data for PT. Marizarasa Sarimurni 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.