AromaProduct Ltd
⚠️ Moderate Risk
FEI: 3009999915 • Tbilisi, Tbilisi • GEORGIA
FEI Number
3009999915
Location
Tbilisi, Tbilisi
Country
GEORGIAAddress
Guramishvili Ave. 17, , Tbilisi, Tbilisi, Georgia
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
JUICE %
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 the food purports to be a beverage containing vegetable or fruit juice and does not bear a statement on the label in appropriate prominence on the information panel of the total percentage of such fruit or vegetable juice contained therein.
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).
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.
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.
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.
LACKS N/C
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)(2) of the FD&C Act in that the food is in package form and the label fails to bear an accurate statement of the quantity of the contents in terms of weight, measure, or numerical count in accordance with Section 403(e)(2) of the FD&C Act.
OFF ODOR
The article appears to consist in whole or in part of a filthy, putrid, or decomposed substance or be otherwise unfit for food. Contains an off odor.
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.
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.
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.
PESTICIDE
The article is subject to refusal of admission pursuant to Section 801(a)(3) in that it appears to bear or contain a pesticide chemical residue, which causes the article to be adulterated within the meaning of section 402(a)(2)(B) of the FD&C Act. Bears or contains:
Refusal History
| Date | Product | Violations | Division |
|---|---|---|---|
| 4/10/2012 | 22KCO01POMEGRANATE, JUICE, OTHER FRUIT JUICES OR CONCENTRATES | New York District Office (NYK-DO) | |
| 4/10/2012 | 22KCO01POMEGRANATE, JUICE, OTHER FRUIT JUICES OR CONCENTRATES | New York District Office (NYK-DO) | |
| 4/10/2012 | 22KCO01POMEGRANATE, JUICE, OTHER FRUIT JUICES OR CONCENTRATES | New York District Office (NYK-DO) | |
| 4/10/2012 | 22KCO01POMEGRANATE, JUICE, OTHER FRUIT JUICES OR CONCENTRATES | New York District Office (NYK-DO) | |
| 4/10/2012 | 22KCO01POMEGRANATE, JUICE, OTHER FRUIT JUICES OR CONCENTRATES | New York District Office (NYK-DO) | |
| 4/10/2012 | 22KCO01POMEGRANATE, JUICE, OTHER FRUIT JUICES OR CONCENTRATES | New York District Office (NYK-DO) | |
| 4/10/2012 | 22KCO01POMEGRANATE, JUICE, OTHER FRUIT JUICES OR CONCENTRATES | New York District Office (NYK-DO) | |
| 4/10/2012 | 22KCO01POMEGRANATE, JUICE, OTHER FRUIT JUICES OR CONCENTRATES | New York District Office (NYK-DO) | |
| 4/28/2011 | 22KCT01POMEGRANATE, JUICE, OTHER FRUIT JUICES OR CONCENTRATES | New York District Office (NYK-DO) | |
| 2/24/2009 | 37JCT03CHILI SAUCE | Seattle District Office (SEA-DO) | |
| 9/10/2004 | 22KCT01POMEGRANATE, JUICE, OTHER FRUIT JUICES OR CONCENTRATES | 241PESTICIDE | New York District Office (NYK-DO) |
Frequently Asked Questions
What is AromaProduct Ltd's FDA import refusal history?
AromaProduct Ltd (FEI: 3009999915) has 11 FDA import refusal record(s) in our database, spanning from 9/10/2004 to 4/10/2012.
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. AromaProduct Ltd's FEI number is 3009999915.
What types of violations has AromaProduct Ltd received?
AromaProduct Ltd has been cited for 12 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 AromaProduct Ltd come from?
All FDA import refusal data for AromaProduct Ltd 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.