Upack Product Ltd
⚠️ Moderate Risk
FEI: 3008260481 • Samara, Samarskaya obl • RUSSIA
FEI Number
3008260481
Location
Samara, Samarskaya obl
Country
RUSSIAAddress
A/Ya 4127, , Samara, Samarskaya 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
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 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)).
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.
ALLERGEN
the label fails to declare all major food allergens present in the product, as required by section 403(w)(1).
TRANSFAT
The product is misbranded under Section 403(q) because the nutrition label does not provide all of the information required by 21 CFR 101.9(c); specifically, the label does not bear the amount of trans fat [21 CFR 101.9(c)(2)(ii)].
LABELING
The article appears in violation of FPLA because of its placement, form and/or contents statement.
Refusal History
| Date | Product | Violations | Division |
|---|---|---|---|
| 1/6/2012 | 07BET05POPCORN, POPPED, FRIED | New York District Office (NYK-DO) | |
| 1/7/2011 | 07BGT02CORN CHIPS, FRIED | New York District Office (NYK-DO) | |
| 1/7/2011 | 07BGT02CORN CHIPS, FRIED | New York District Office (NYK-DO) | |
| 5/18/2010 | 07AGT05POPCORN, POPPED, BAKED | New York District Office (NYK-DO) | |
| 5/18/2010 | 07AGT05POPCORN, POPPED, BAKED | New York District Office (NYK-DO) | |
| 5/18/2010 | 07AGT05POPCORN, POPPED, BAKED | New York District Office (NYK-DO) |
Frequently Asked Questions
What is Upack Product Ltd's FDA import refusal history?
Upack Product Ltd (FEI: 3008260481) has 6 FDA import refusal record(s) in our database, spanning from 5/18/2010 to 1/6/2012.
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. Upack Product Ltd's FEI number is 3008260481.
What types of violations has Upack Product Ltd received?
Upack Product Ltd 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 Upack Product Ltd come from?
All FDA import refusal data for Upack Product 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.