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PT. Meka Permata Rejeki

⚠️ Moderate Risk

FEI: 2000044392 • Benoa-Denpasar, Bali • INDONESIA

FEI

FEI Number

2000044392

📍

Location

Benoa-Denpasar, Bali

🇮🇩

Country

INDONESIA
🏢

Address

Jalan Ikan Tuna Raya No. 17, , Benoa-Denpasar, Bali, Indonesia

Moderate Risk

FDA Import Risk Assessment

48.6
LowModerateHighCritical

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

Statistics

7
Total Refusals
2
Unique Violations
10/3/2007
Latest Refusal
10/3/2007
Earliest Refusal

Score Breakdown

Violation Severity
78.9×40%
Refusal Volume
33.5×30%
Recency
0.0×20%
Frequency
70.0×10%
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

23607×

HISTAMINE

The article appears to bear or contain histamine, a poisonous and deleterious substance in such quantity as ordinarily renders it 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.

Refusal History

DateProductViolationsDivision
10/3/2007
16AGT45TUNA (ALBACORE, YELLOWFIN, BLUEFIN, SKIPJACK, ETC.)
2360HISTAMINE
Los Angeles District Office (LOS-DO)
10/3/2007
16AGT45TUNA (ALBACORE, YELLOWFIN, BLUEFIN, SKIPJACK, ETC.)
2360HISTAMINE
Los Angeles District Office (LOS-DO)
10/3/2007
16AGT45TUNA (ALBACORE, YELLOWFIN, BLUEFIN, SKIPJACK, ETC.)
2360HISTAMINE
Los Angeles District Office (LOS-DO)
10/3/2007
16AGT45TUNA (ALBACORE, YELLOWFIN, BLUEFIN, SKIPJACK, ETC.)
2360HISTAMINE
Los Angeles District Office (LOS-DO)
10/3/2007
16AGT45TUNA (ALBACORE, YELLOWFIN, BLUEFIN, SKIPJACK, ETC.)
2360HISTAMINE
Los Angeles District Office (LOS-DO)
10/3/2007
16AGT45TUNA (ALBACORE, YELLOWFIN, BLUEFIN, SKIPJACK, ETC.)
218LIST INGRE
2360HISTAMINE
Los Angeles District Office (LOS-DO)
10/3/2007
16AGT45TUNA (ALBACORE, YELLOWFIN, BLUEFIN, SKIPJACK, ETC.)
218LIST INGRE
2360HISTAMINE
Los Angeles District Office (LOS-DO)

Frequently Asked Questions

What is PT. Meka Permata Rejeki's FDA import refusal history?

PT. Meka Permata Rejeki (FEI: 2000044392) has 7 FDA import refusal record(s) in our database, spanning from 10/3/2007 to 10/3/2007.

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. Meka Permata Rejeki's FEI number is 2000044392.

What types of violations has PT. Meka Permata Rejeki received?

PT. Meka Permata Rejeki has been cited for 2 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. Meka Permata Rejeki come from?

All FDA import refusal data for PT. Meka Permata Rejeki 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.