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Udaan International

⚠️ Moderate Risk

FEI: 3012318734 • Ahmedabad, Gujarat • INDIA

FEI

FEI Number

3012318734

📍

Location

Ahmedabad, Gujarat

🇮🇳

Country

INDIA
🏢

Address

Maruti Co Op Society, Near Old Water Tank, Ahmedabad, Gujarat, India

Moderate Risk

FDA Import Risk Assessment

37.2
LowModerateHighCritical

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

Statistics

8
Total Refusals
12
Unique Violations
11/30/2020
Latest Refusal
7/12/2017
Earliest Refusal

Score Breakdown

Violation Severity
60.6×40%
Refusal Volume
35.3×30%
Recency
0.0×20%
Frequency
23.6×10%
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

1183×

NOT LISTED

It appears the drug or device is not included in a list required by Section 510(j), or a notice or other information respecting it was not provided as required by section 510(j) or 510(k).

2493×

FILTHY

The article is subject to refusal of admission pursuant to Section 801(a)(3) in that the article appears to consist in whole or in part of a filthy, putrid, or decomposed substance or be otherwise unfit for food.

4822×

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.

752×

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).

111×

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).

3411×

REGISTERED

It appears the device is subject to listing under 510(j) and the initial distributor has not registered as required by 21 CFR 807.20 (a)(5).

4731×

LABELING

The article appears in violation of FPLA because of its placement, form and/or contents statement.

641×

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.

32801×

FRNMFGREG

The article is subject to refusal of admission pursuant to section 801(a)(3) in that it appears to be misbranded as defined in section 502(o) of the FD&C Act. It appears that it was manufactured, prepared, propagated, compounded, or processed in an establishment not duly registered under section 510 of the Act.

2181×

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.

2761×

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.

3201×

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.

Refusal History

DateProductViolationsDivision
11/30/2020
30FGY99BEVERAGE BASE OF NON-FRUIT ORIGIN, N.E.C.
320LACKS FIRM
482NUTRIT LBL
Division of Northeast Imports (DNEI)
9/16/2019
76EFWTOOTHBRUSH, MANUAL
118NOT LISTED
3280FRNMFGREG
341REGISTERED
Division of Northeast Imports (DNEI)
4/20/2018
66FAY99SUPPRESSANT N.E.C.
118NOT LISTED
75UNAPPROVED
Division of Northeast Imports (DNEI)
4/20/2018
66FAY99SUPPRESSANT N.E.C.
118NOT LISTED
75UNAPPROVED
Division of Northeast Imports (DNEI)
2/20/2018
35AGT99GELATIN, N.E.C.
11UNSAFE COL
218LIST INGRE
276PRESRV LBL
473LABELING
482NUTRIT LBL
64YELLOW #5
Division of Northeast Imports (DNEI)
7/12/2017
03YGY99OTHER BAKERY PRODUCTS, N.E.C.
249FILTHY
Division of Northeast Imports (DNEI)
7/12/2017
03YGY99OTHER BAKERY PRODUCTS, N.E.C.
249FILTHY
Division of Northeast Imports (DNEI)
7/12/2017
03YGY99OTHER BAKERY PRODUCTS, N.E.C.
249FILTHY
Division of Northeast Imports (DNEI)

Frequently Asked Questions

What is Udaan International's FDA import refusal history?

Udaan International (FEI: 3012318734) has 8 FDA import refusal record(s) in our database, spanning from 7/12/2017 to 11/30/2020.

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. Udaan International's FEI number is 3012318734.

What types of violations has Udaan International received?

Udaan International has been cited for 12 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 Udaan International come from?

All FDA import refusal data for Udaan 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.