ImportRefusal LogoImportRefusal

ALOE PLUS INTERNATIONAL

⚠️ Moderate Risk

FEI: 3010586942 • Mumbai, Maharashtra • INDIA

FEI

FEI Number

3010586942

📍

Location

Mumbai, Maharashtra

🇮🇳

Country

INDIA
🏢

Address

225 Aarey Colony Road, , Mumbai, Maharashtra, India

Moderate Risk

FDA Import Risk Assessment

48.3
LowModerateHighCritical

This firm has a moderate history of FDA import refusals. Some attention may be warranted.

Statistics

15
Total Refusals
7
Unique Violations
6/4/2015
Latest Refusal
6/4/2015
Earliest Refusal

Score Breakdown

Violation Severity
62.4×40%
Refusal Volume
44.6×30%
Recency
0.0×20%
Frequency
100.0×10%
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

7510×

UNAPPROVED

The article is subject to refusal of admission pursuant to Section 801(a)(3) in that it appears to be a new drug within the meaning of Section 201(p) without an approved New Drug Application (NDA).

4824×

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.

2604×

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.

3213×

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.

2762×

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.

37211×

PESTICIDE2

The article is subject to refusal of admission pursuant to section 801(a)(3) in that it appears to be adulterated because it contains a pesticide chemical, which is in violation of section 402(a)(2)(B). Contains:

23001×

DIETARYLBL

The article is subject to refusal of admission pursuant to Section 801(a)(3) of the FD&C Act in that it is a dietary supplement that appears to be misbranded within the meaning of Section 403(s)(2)(B) of the FD&C Act in that the label or labeling fails to identify the product by using the term "dietary supplement", which term may be modified with the name of such an ingredient.

Refusal History

DateProductViolationsDivision
6/4/2015
29YGT99SOFT DRINKS AND WATERS NOT MENTIONED ELSEWHERE, N.E.C.
2300DIETARYLBL
482NUTRIT LBL
Division of Northern Border Imports (DNBI)
6/4/2015
29YGT99SOFT DRINKS AND WATERS NOT MENTIONED ELSEWHERE, N.E.C.
260FALSE
3721PESTICIDE2
Division of Northern Border Imports (DNBI)
6/4/2015
33LFT07JELLIED CANDY, SOFT (JELLY BEANS, GUM DROPS, ETC.), WITHOUT NUTS AND FRUIT (WITHOUT CHOCOLATE)
260FALSE
321LACKS N/C
482NUTRIT LBL
Division of Northern Border Imports (DNBI)
6/4/2015
33LFT07JELLIED CANDY, SOFT (JELLY BEANS, GUM DROPS, ETC.), WITHOUT NUTS AND FRUIT (WITHOUT CHOCOLATE)
260FALSE
276PRESRV LBL
321LACKS N/C
482NUTRIT LBL
Division of Northern Border Imports (DNBI)
6/4/2015
33LFT07JELLIED CANDY, SOFT (JELLY BEANS, GUM DROPS, ETC.), WITHOUT NUTS AND FRUIT (WITHOUT CHOCOLATE)
260FALSE
276PRESRV LBL
321LACKS N/C
482NUTRIT LBL
Division of Northern Border Imports (DNBI)
6/4/2015
29YGT99SOFT DRINKS AND WATERS NOT MENTIONED ELSEWHERE, N.E.C.
75UNAPPROVED
Division of Northern Border Imports (DNBI)
6/4/2015
29YGT99SOFT DRINKS AND WATERS NOT MENTIONED ELSEWHERE, N.E.C.
75UNAPPROVED
Division of Northern Border Imports (DNBI)
6/4/2015
29YGT99SOFT DRINKS AND WATERS NOT MENTIONED ELSEWHERE, N.E.C.
75UNAPPROVED
Division of Northern Border Imports (DNBI)
6/4/2015
29YGT99SOFT DRINKS AND WATERS NOT MENTIONED ELSEWHERE, N.E.C.
75UNAPPROVED
Division of Northern Border Imports (DNBI)
6/4/2015
29YGT99SOFT DRINKS AND WATERS NOT MENTIONED ELSEWHERE, N.E.C.
75UNAPPROVED
Division of Northern Border Imports (DNBI)
6/4/2015
29YGT99SOFT DRINKS AND WATERS NOT MENTIONED ELSEWHERE, N.E.C.
75UNAPPROVED
Division of Northern Border Imports (DNBI)
6/4/2015
29YGT99SOFT DRINKS AND WATERS NOT MENTIONED ELSEWHERE, N.E.C.
75UNAPPROVED
Division of Northern Border Imports (DNBI)
6/4/2015
29YGT99SOFT DRINKS AND WATERS NOT MENTIONED ELSEWHERE, N.E.C.
75UNAPPROVED
Division of Northern Border Imports (DNBI)
6/4/2015
29YGT99SOFT DRINKS AND WATERS NOT MENTIONED ELSEWHERE, N.E.C.
75UNAPPROVED
Division of Northern Border Imports (DNBI)
6/4/2015
29YGT99SOFT DRINKS AND WATERS NOT MENTIONED ELSEWHERE, N.E.C.
75UNAPPROVED
Division of Northern Border Imports (DNBI)

Frequently Asked Questions

What is ALOE PLUS INTERNATIONAL's FDA import refusal history?

ALOE PLUS INTERNATIONAL (FEI: 3010586942) has 15 FDA import refusal record(s) in our database, spanning from 6/4/2015 to 6/4/2015.

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. ALOE PLUS INTERNATIONAL's FEI number is 3010586942.

What types of violations has ALOE PLUS INTERNATIONAL received?

ALOE PLUS INTERNATIONAL 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 ALOE PLUS INTERNATIONAL come from?

All FDA import refusal data for ALOE PLUS INTERNATIONAL 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.