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PT.WIRA AKSARA

⚠️ Moderate Risk

FEI: 3009826685 • Jakarta Selatan, Jabotabek • INDONESIA

FEI

FEI Number

3009826685

📍

Location

Jakarta Selatan, Jabotabek

🇮🇩

Country

INDONESIA
🏢

Address

Jl. Mpr 1/17, , Jakarta Selatan, Jabotabek, Indonesia

Moderate Risk

FDA Import Risk Assessment

46.3
LowModerateHighCritical

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

Statistics

17
Total Refusals
10
Unique Violations
5/9/2018
Latest Refusal
8/17/2004
Earliest Refusal

Score Breakdown

Violation Severity
77.7×40%
Refusal Volume
46.5×30%
Recency
0.0×20%
Frequency
12.4×10%
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

24910×

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.

93×

SALMONELLA

The article is subject to refusal of admission pursuant to Section 801(a)(3) in that it appears to contain Salmonella, a poisonous and deleterious substance which may render it injurious to health.

3283×

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.

2742×

COLOR LBLG

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

832×

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.

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.

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.

3061×

INSANITARY

The article is subject to refusal of admission pursuant to Section 801(a)(3) in that it appears to have been prepared, packed, or held under insanitary conditions whereby it may have become contaminated with filth, or whereby it may have been rendered injurious to health.

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).

Refusal History

DateProductViolationsDivision
5/9/2018
28AGH05BAY (LAUREL), WHOLE (SPICE)
9SALMONELLA
Division of West Coast Imports (DWCI)
5/15/2017
36AFT99SUGAR PRODUCTS, N.E.C.
249FILTHY
Division of Northern Border Imports (DNBI)
3/18/2016
28AGH05BAY (LAUREL), WHOLE (SPICE)
9SALMONELLA
Los Angeles District Office (LOS-DO)
9/11/2013
02HGT01TAPIOCA STARCH PRODUCT
274COLOR LBLG
Los Angeles District Office (LOS-DO)
6/19/2009
02HGT01TAPIOCA STARCH PRODUCT
11UNSAFE COL
274COLOR LBLG
64YELLOW #5
Los Angeles District Office (LOS-DO)
5/5/2008
36AGT03CANE SUGAR (SUCROSE)
249FILTHY
328USUAL NAME
482NUTRIT LBL
Los Angeles District Office (LOS-DO)
12/27/2007
36AGT03CANE SUGAR (SUCROSE)
249FILTHY
Los Angeles District Office (LOS-DO)
12/27/2007
36AGT03CANE SUGAR (SUCROSE)
249FILTHY
Los Angeles District Office (LOS-DO)
8/8/2007
36AGT03CANE SUGAR (SUCROSE)
249FILTHY
Los Angeles District Office (LOS-DO)
1/22/2007
36AHT99SUGAR PRODUCTS, N.E.C.
249FILTHY
Los Angeles District Office (LOS-DO)
11/22/2006
36AGT03CANE SUGAR (SUCROSE)
249FILTHY
306INSANITARY
Los Angeles District Office (LOS-DO)
11/22/2006
36AGT03CANE SUGAR (SUCROSE)
249FILTHY
Los Angeles District Office (LOS-DO)
11/22/2006
36AGT03CANE SUGAR (SUCROSE)
218LIST INGRE
249FILTHY
328USUAL NAME
Los Angeles District Office (LOS-DO)
11/22/2006
36AGT03CANE SUGAR (SUCROSE)
218LIST INGRE
249FILTHY
328USUAL NAME
Los Angeles District Office (LOS-DO)
8/21/2006
37JCE05SOY SAUCE
83NO PROCESS
Los Angeles District Office (LOS-DO)
8/21/2006
37JCE05SOY SAUCE
83NO PROCESS
Los Angeles District Office (LOS-DO)
8/17/2004
16AGH36SMELT
9SALMONELLA
Los Angeles District Office (LOS-DO)

Frequently Asked Questions

What is PT.WIRA AKSARA's FDA import refusal history?

PT.WIRA AKSARA (FEI: 3009826685) has 17 FDA import refusal record(s) in our database, spanning from 8/17/2004 to 5/9/2018.

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.WIRA AKSARA's FEI number is 3009826685.

What types of violations has PT.WIRA AKSARA received?

PT.WIRA AKSARA has been cited for 10 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.WIRA AKSARA come from?

All FDA import refusal data for PT.WIRA AKSARA 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.