Artashes LLC
⚠️ Moderate Risk
FEI: 3012888246 • Abovyan, Kotayki • ARMENIA
FEI Number
3012888246
Location
Abovyan, Kotayki
Country
ARMENIAAddress
5 Barekamutyan, , Abovyan, Kotayki, Armenia
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
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.
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.
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.
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.
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.
UNSAFE ADD
The article is subject to refusal of admission pursuant to Section 801(a)(3) in that it appears to bear or contain an unsafe food additive within the meaning of section 409.
CHLORAMP
The article appears to contain a food additive, namely chloramphenicol, that is unsafe within the meaning of 21 U.S.C. 348.
NITROFURAN
The article is subject to refusal of admission in that it appears to bear or contain a food additive, namely nitrofurans, that is unsafe.
Refusal History
| Date | Product | Violations | Division |
|---|---|---|---|
| 8/15/2016 | 36CCT04HONEY | Los Angeles District Office (LOS-DO) | |
| 1/31/2005 | 25ECE99MIXED VEGETABLES, N.E.C. | 83NO PROCESS | Los Angeles District Office (LOS-DO) |
| 4/3/2002 | 21UCN03FIG, JAM, JELLY, PRESERVES, MARMALADE, BUTTER OR CANDIED | Los Angeles District Office (LOS-DO) | |
| 4/3/2002 | 20CCN03BOYSENBERRY, JAM, JELLY, PRESERVES, MARMALADE, BUTTER AND CANDIED | Los Angeles District Office (LOS-DO) |
Frequently Asked Questions
What is Artashes LLC's FDA import refusal history?
Artashes LLC (FEI: 3012888246) has 4 FDA import refusal record(s) in our database, spanning from 4/3/2002 to 8/15/2016.
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. Artashes LLC's FEI number is 3012888246.
What types of violations has Artashes LLC received?
Artashes LLC has been cited for 8 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 Artashes LLC come from?
All FDA import refusal data for Artashes LLC 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.