STAR GREENFALL
⚠️ Moderate Risk
FEI: 3016195908 • Sukoharjo, Jawa Tengah • INDONESIA
FEI Number
3016195908
Location
Sukoharjo, Jawa Tengah
Country
INDONESIAAddress
Manang,Grogol, Jln. Sidomulyo 1, Sukoharjo, Jawa Tengah, Indonesia
Moderate Risk
FDA Import Risk Assessment
This firm has a moderate history of FDA import refusals. Some attention may be warranted.
Statistics
Score Breakdown
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
POISONOUS
The article is subject to refusal of admission pursuant to Section 801(a)(3) in that it appears to bear or contain a poisonous or deleterious substance which may render the article injurious to health. Contains:
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.
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.
LACKS FIRM
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(e)(1) of the FD&C Act in that the food is in package form and the label fails to bear the name and place of business of the manufacturer, packer, or distributor.
NO ENGLISH
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(f) of the FD&C Act in that any word, statement, or other information required by or under the authority of the FD&C Act to appear on the label or labeling is not prominently placed thereon with such conspicuousness (as compared with other words, statements, designs, or devices, in the labeling) and in such terms as to render it likely to be read and understood by the ordinary individual under customary terms of purchase and use (for example, label contains information in two or more languages but fails to repeat all required information in both languages in accordance with 21 CFR 101.15(c)(2), or label fails to include all required information in English in accordance with 21 CFR 101.15(c)(1), except in the case of articles distributed solely in the Commonwealth of Puerto Rico or in a Territory where the predominant language is one other than English)).
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.
Refusal History
| Date | Product | Violations | Division |
|---|---|---|---|
| 2/7/2020 | 54JYY12KRATOM (HERBAL AND BOTANICAL TEAS II, CONTINUED) | Division of Southeast Imports (DSEI) | |
| 2/7/2020 | 31AYT99COFFEE, N.E.C. | 324NO ENGLISH | Division of Southeast Imports (DSEI) |
| 2/6/2020 | 54JYR11BETEL NUT (HERBAL AND BOTANICAL TEAS II, CONTINUED) | Division of Southeast Imports (DSEI) | |
| 1/31/2020 | 54KYY09BETEL LEAF (HERBAL AND BOTANICAL (NOT TEAS) II (CONTINUED)) | 251POISONOUS | Division of Southeast Imports (DSEI) |
Frequently Asked Questions
What is STAR GREENFALL's FDA import refusal history?
STAR GREENFALL (FEI: 3016195908) has 4 FDA import refusal record(s) in our database, spanning from 1/31/2020 to 2/7/2020.
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. STAR GREENFALL's FEI number is 3016195908.
What types of violations has STAR GREENFALL received?
STAR GREENFALL has been cited for 6 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 STAR GREENFALL come from?
All FDA import refusal data for STAR GREENFALL 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.