Abo Draa Est.
⚠️ Moderate Risk
FEI: 3005343432 • Saida • LEBANON
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
LABELING
The article appears in violation of FPLA because of its placement, form and/or contents statement.
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.
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).
YELLOW #5
The food appears to bear or contain the color additive FD & C Yellow No. 5, which is not declared on the label per 21 CFR 74.705(a)(c) under section 721.
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.
USUAL NAME
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)(1) of the FD&C Act in that the label fails to bear the common or usual name of the food, if any there be.
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)].
Refusal History
| Date | Product | Violations | Division |
|---|---|---|---|
| 10/24/2007 | 33UGT01BUBBLE GUM (WITHOUT CHOCOLATE) | Detroit District Office (DET-DO) | |
| 10/24/2007 | 34FGT01CHOCOLATE CANDY BAR, WITHOUT NUTS AND FRUIT | Detroit District Office (DET-DO) | |
| 10/24/2007 | 29WGT02BOTTLED SPRING OR MINERAL WATER | Detroit District Office (DET-DO) | |
| 10/24/2007 | 33LGT05CANDY BAR OR PIECES (NOT CARAMEL OR FONDANT), SOFT, WITHOUT NUTS AND FRUIT (WITHOUT CHOCOLATE) | Detroit District Office (DET-DO) | |
| 10/24/2007 | 33UGT02CHEWING GUM (WITHOUT CHOCOLATE) | Detroit District Office (DET-DO) | |
| 10/24/2007 | 33LGT03FONDANT CANDY BAR, SOFT, WITHOUT NUTS AND FRUIT (WITHOUT CHOCOLATE) | Detroit District Office (DET-DO) | |
| 10/24/2007 | 33EGT06FLAVORED CANDY, HARD (LIVE SAVERS, ETC.), WITHOUT NUTS AND FRUIT (WITHOUT CHOCOLATE) | Detroit District Office (DET-DO) |
Frequently Asked Questions
What is Abo Draa Est.'s FDA import refusal history?
Abo Draa Est. (FEI: 3005343432) has 7 FDA import refusal record(s) in our database, spanning from 10/24/2007 to 10/24/2007.
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. Abo Draa Est.'s FEI number is 3005343432.
What types of violations has Abo Draa Est. received?
Abo Draa Est. 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 Abo Draa Est. come from?
All FDA import refusal data for Abo Draa Est. 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.