Litex Juice Jsco
⚠️ Moderate Risk
FEI: 3003863378 • Lovech, Lovech • BULGARIA
FEI Number
3003863378
Location
Lovech, Lovech
Country
BULGARIAAddress
Targovska Str 12, , Lovech, Lovech, Bulgaria
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
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.
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.
FALSE
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(a)(1 ) of the FD&C Act in that the labeling is false or misleading in any particular.
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.
Refusal History
| Date | Product | Violations | Division |
|---|---|---|---|
| 7/7/2004 | 20SDF01APPLE, CORE FRUIT JUICES OR CONCENTRATES | 260FALSE | San Francisco District Office (SAN-DO) |
| 7/7/2004 | 21ADF03BERRIES, MIXED | San Francisco District Office (SAN-DO) | |
| 5/15/2003 | 30PDF03BEVERAGE BASE, COMBINATION TRUE FRUIT AND IMITATION FRUIT FLAVORS, LIQUID (NOT COCKTAIL OR PUNCH) | San Francisco District Office (SAN-DO) | |
| 5/9/2003 | 30PDF03BEVERAGE BASE, COMBINATION TRUE FRUIT AND IMITATION FRUIT FLAVORS, LIQUID (NOT COCKTAIL OR PUNCH) | San Francisco District Office (SAN-DO) |
Frequently Asked Questions
What is Litex Juice Jsco's FDA import refusal history?
Litex Juice Jsco (FEI: 3003863378) has 4 FDA import refusal record(s) in our database, spanning from 5/9/2003 to 7/7/2004.
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. Litex Juice Jsco's FEI number is 3003863378.
What types of violations has Litex Juice Jsco received?
Litex Juice Jsco has been cited for 5 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 Litex Juice Jsco come from?
All FDA import refusal data for Litex Juice Jsco 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.