Aqualife PK
⚠️ Moderate Risk
FEI: 3011424588 • Yamkino, Moskovskaya obl • RUSSIA
FEI Number
3011424588
Location
Yamkino, Moskovskaya obl
Country
RUSSIAAddress
2, Building 1, Industrial Zone Noginsk 2, , Yamkino, Moskovskaya obl, Russia
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
UNSAFE COL
The article appears to be, or to bear or contain a color additive which is unsafe within the meaning of Section 721(a).
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.
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.
PRESRV LBL
The article is subject to refusal of admission pursuant to Section 801(a)(3) in that it appears to contain a chemical preservative and it fails to bear labeling stating that fact including its function.
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.
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.
ALLERGEN
the label fails to declare all major food allergens present in the product, as required by section 403(w)(1).
Refusal History
| Date | Product | Violations | Division |
|---|---|---|---|
| 4/12/2018 | 29BET99CARBONATED SOFT DRINK, N.E.C. | 249FILTHY | Division of Northeast Imports (DNEI) |
| 9/19/2016 | 29BGT06SOFT DRINK, IMITATION FRUIT FLAVORED, CARBONATED | San Francisco District Office (SAN-DO) | |
| 8/2/2012 | 29BGT99CARBONATED SOFT DRINK, N.E.C. | 11UNSAFE COL | Seattle District Office (SEA-DO) |
| 8/2/2012 | 29BCT99CARBONATED SOFT DRINK, N.E.C. | 11UNSAFE COL | Seattle District Office (SEA-DO) |
| 8/2/2012 | 29BCT99CARBONATED SOFT DRINK, N.E.C. | 11UNSAFE COL | Seattle District Office (SEA-DO) |
Frequently Asked Questions
What is Aqualife PK's FDA import refusal history?
Aqualife PK (FEI: 3011424588) has 5 FDA import refusal record(s) in our database, spanning from 8/2/2012 to 4/12/2018.
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. Aqualife PK's FEI number is 3011424588.
What types of violations has Aqualife PK received?
Aqualife PK has been cited for 7 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 Aqualife PK come from?
All FDA import refusal data for Aqualife PK 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.