MAX INTERNATIONAL COMPANY
⚠️ High Risk
FEI: 3005340410 • Ajman, Ajman • UNITED ARAB EMIRATES
FEI Number
3005340410
Location
Ajman, Ajman
Country
UNITED ARAB EMIRATESAddress
Ajman Free Zone, Gate #3 # A7; Land, Ajman, Ajman, United Arab Emirates
High Risk
FDA Import Risk Assessment
This firm has a significant history of FDA import refusals with notable violations.
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
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.
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).
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.
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.
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.
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.
MFR INSAN
The article is subject to refusal of admission pursuant to section 801(a)(1) in that the article appears to have been manufactured, processed, or packed under insanitary conditions.
BACTERIA
The article appears to contain a poisonous and deleterious substance which may render it injurious to health. Contains
Refusal History
| Date | Product | Violations | Division |
|---|---|---|---|
| 10/17/2007 | 29WCT01BOTTLED WATER | Los Angeles District Office (LOS-DO) | |
| 10/16/2007 | 29WCT01BOTTLED WATER | Los Angeles District Office (LOS-DO) | |
| 10/16/2007 | 29WCT01BOTTLED WATER | Los Angeles District Office (LOS-DO) | |
| 10/16/2007 | 29WCT01BOTTLED WATER | Los Angeles District Office (LOS-DO) | |
| 10/16/2007 | 29WCT01BOTTLED WATER | Los Angeles District Office (LOS-DO) | |
| 10/16/2007 | 29WCT01BOTTLED WATER | Los Angeles District Office (LOS-DO) | |
| 10/16/2007 | 29WCT01BOTTLED WATER | Los Angeles District Office (LOS-DO) | |
| 10/16/2007 | 29WCT01BOTTLED WATER | Los Angeles District Office (LOS-DO) | |
| 10/16/2007 | 29WCT01BOTTLED WATER | Los Angeles District Office (LOS-DO) | |
| 10/16/2007 | 29WCT01BOTTLED WATER | Los Angeles District Office (LOS-DO) | |
| 10/3/2007 | 29WCT01BOTTLED WATER | Los Angeles District Office (LOS-DO) |
Frequently Asked Questions
What is MAX INTERNATIONAL COMPANY's FDA import refusal history?
MAX INTERNATIONAL COMPANY (FEI: 3005340410) has 11 FDA import refusal record(s) in our database, spanning from 10/3/2007 to 10/17/2007.
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. MAX INTERNATIONAL COMPANY's FEI number is 3005340410.
What types of violations has MAX INTERNATIONAL COMPANY received?
MAX INTERNATIONAL COMPANY has been cited for 9 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 MAX INTERNATIONAL COMPANY come from?
All FDA import refusal data for MAX INTERNATIONAL COMPANY 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.