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Sahruji

⚠️ Moderate Risk

FEI: 3011992123 • Bandung, Jawa Barat • INDONESIA

FEI

FEI Number

3011992123

📍

Location

Bandung, Jawa Barat

🇮🇩

Country

INDONESIA
🏢

Address

Jln. Budi Permai, 45 BANDUNG, Bandung, Jawa Barat, Indonesia

Moderate Risk

FDA Import Risk Assessment

44.2
LowModerateHighCritical

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

Statistics

8
Total Refusals
4
Unique Violations
9/23/2022
Latest Refusal
2/24/2016
Earliest Refusal

Score Breakdown

Violation Severity
71.1×40%
Refusal Volume
35.3×30%
Recency
19.7×20%
Frequency
12.2×10%
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

21206×

UNSFDIETSP

The article appears to be a dietary supplement or ingredient for which there is inadequate information to provide reasonable assurance that such ingredient does not present a significant or unreasonable risk of illness or injury.

161×

DIRECTIONS

The article is subject to refusal of admission pursuant to section 801(a)(3) in that it is a device whose label appears to not bear adequate directions for use.

2181×

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.

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.

Refusal History

DateProductViolationsDivision
9/23/2022
54KYR12KRATOM (HERBAL AND BOTANICALS, NOT TEAS II)
2120UNSFDIETSP
Division of Southeast Imports (DSEI)
4/16/2018
54KBR12KRATOM (HERBAL AND BOTANICALS, NOT TEAS II)
16DIRECTIONS
Division of Southeast Imports (DSEI)
9/20/2016
54JYY12KRATOM (HERBAL AND BOTANICAL TEAS II, CONTINUED)
2120UNSFDIETSP
Division of Southeast Imports (DSEI)
6/28/2016
54KYR12KRATOM (HERBAL AND BOTANICALS, NOT TEAS II)
2120UNSFDIETSP
Cincinnati District Office (CIN-DO)
6/28/2016
54KYR12KRATOM (HERBAL AND BOTANICALS, NOT TEAS II)
2120UNSFDIETSP
Cincinnati District Office (CIN-DO)
6/28/2016
54KYR12KRATOM (HERBAL AND BOTANICALS, NOT TEAS II)
2120UNSFDIETSP
Cincinnati District Office (CIN-DO)
6/21/2016
54KBR12KRATOM (HERBAL AND BOTANICALS, NOT TEAS II)
2120UNSFDIETSP
218LIST INGRE
Cincinnati District Office (CIN-DO)
2/24/2016
54KBR12KRATOM (HERBAL AND BOTANICALS, NOT TEAS II)
260FALSE
Cincinnati District Office (CIN-DO)

Frequently Asked Questions

What is Sahruji's FDA import refusal history?

Sahruji (FEI: 3011992123) has 8 FDA import refusal record(s) in our database, spanning from 2/24/2016 to 9/23/2022.

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. Sahruji's FEI number is 3011992123.

What types of violations has Sahruji received?

Sahruji 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 Sahruji come from?

All FDA import refusal data for Sahruji 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.