Arssi Alliance LLC
FDA import alert and refusal historyYerevan, ArmeniaFEI 3013122646
Recorded by FDA as ARSSI ALLIANCE LLC
As of October 26, 2026, Arssi Alliance LLC (Yerevan, Armenia) is on the red list of FDA Import Alert 45-02 (Foods with illegal or undeclared colors) for immune booster antiviral, published by FDA on August 25, 2023, is also listed on Import Alert 99-39 (red list), and has 1 FDA import refusal recorded since October 2016.
Data from FDA public records, last checked . Request a correction
Current status
- Import alerts
- IA 45-02 · red listIA 99-39 · red list
- Last import refusal
- Vitamin, mineral, proteins and unconventional dietary specialities for humans and animals, n.e.c. · LIST INGRE
- Last warning letter
- None found
- Last inspection
- None on record
Every FDA record for Arssi Alliance LLC
3 records, newest first. Each line links to the FDA page it came from.
2023
- Import alert listingListed on Import Alert 45-02red listImmune booster antiviralSource
- Import alert listingListed on Import Alert 99-39red listImmune Booster AntiviralSource
- Import refusalRefused, Vitamin, mineral, proteins and unconventional dietary specialities for humans and animals, n.e.c.LIST INGREDIETARYLBLUNSAFE COLPLANT PARTNCONTACTNUTRIT LBLUNAPPROVEDEntry BWS-0004130-4Source
Refusal charges, in plain English
- DIETARYLBL1 refused line
Not identified as a dietary supplement
The label appeared not to identify the product with the term "dietary supplement" (which may be modified with the name of an ingredient).
- LIST INGRE1 refused line
Ingredients not listed
The product is made from two or more ingredients and the label appeared not to list the common or usual name of each one (or, for a juice beverage, the percentage of juice).
- NCONTACT1 refused line
No U.S. adverse event contact on supplement label
The dietary supplement label appeared not to show a U.S. address or phone number through which a serious adverse event can be reported.
- NUTRIT LBL1 refused line
Nutrition information missing from label
The label or labeling appeared not to carry the nutrition information that U.S. law requires for the food.
- PLANT PART1 refused line
PLANT PART
- UNAPPROVED1 refused line
Unapproved new drug
The product appeared to be a new drug within the meaning of section 201(p) of the FD&C Act without an approved New Drug Application. FDA can apply this charge to a food or supplement whose labeling presents it for drug uses.
- UNSAFE COL1 refused line
Color additive unsafe under section 721
The product appeared to be, or to contain, a color additive that is unsafe within the meaning of section 721(a) of the FD&C Act, the section that governs which color additives may be used and how.
Questions about Arssi Alliance LLC
- Is Arssi Alliance LLC on an FDA import alert?
- Yes. As of October 26, 2026, Arssi Alliance LLC is on the red list of FDA Import Alert 45-02, “Foods with illegal or undeclared colors”, for immune booster antiviral; FDA published the listing on August 25, 2023.
- Has FDA refused shipments from Arssi Alliance LLC?
- Yes. FDA refused 1 shipment line from Arssi Alliance LLC on August 18, 2023. The most recent, on August 18, 2023, was vitamin, mineral, proteins and unconventional dietary specialities for humans and animals, n.e.c., charged as LIST INGRE (ingredients not listed).
- Why did FDA refuse Arssi Alliance LLC's shipments?
- The most frequent charges are DIETARYLBL (not identified as a dietary supplement, 1 line) and LIST INGRE (ingredients not listed, 1 line).
- What is Arssi Alliance LLC's FEI number?
- Arssi Alliance LLC's FDA Establishment Identifier (FEI) is 3013122646.
- Can shipments from Arssi Alliance LLC still enter the U.S.?
- Shipments of immune booster antiviral from Arssi Alliance LLC can be detained without physical examination under Import Alert 45-02; FDA releases them only if evidence shows they do not have the listed violation. Importers must consider this listing in their FSVP evaluation (21 CFR 1.505).
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SupplierRadar is not affiliated with the U.S. Food and Drug Administration. Data comes from public FDA records and may contain errors. This is not legal advice; importers remain responsible for their supplier evaluations.