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HIMALYA INTERNATIONAL LTD.

⚠️ Moderate Risk

FEI: 3004250068 • Shubh Khera, Himachal Pradesh • INDIA

FEI

FEI Number

3004250068

📍

Location

Shubh Khera, Himachal Pradesh

🇮🇳

Country

INDIA
🏢

Address

Paonta Sahib Sahib, Himachal Pradesh, Shubh Khera, Himachal Pradesh, India

Moderate Risk

FDA Import Risk Assessment

39.4
LowModerateHighCritical

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

Statistics

3
Total Refusals
5
Unique Violations
7/16/2015
Latest Refusal
4/28/2011
Earliest Refusal

Score Breakdown

Violation Severity
80.0×40%
Refusal Volume
22.3×30%
Recency
0.0×20%
Frequency
7.1×10%
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

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.

29201×

PESTICIDES

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:

3061×

INSANITARY

The article is subject to refusal of admission pursuant to Section 801(a)(3) in that it appears to have been prepared, packed, or held under insanitary conditions whereby it may have become contaminated with filth, or whereby it may have been rendered injurious to health.

3081×

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.

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:

Refusal History

DateProductViolationsDivision
7/16/2015
25PGN01MUSHROOM, COMMON (AGARICUS BISPORUS), WHOLE (BUTTON) (FUNGI)
218LIST INGRE
3721PESTICIDE2
Baltimore District Office (BLT-DO)
7/12/2013
12AGN09COTTAGE CHEESE DRY CURD(<0.5% MILKFAT)
306INSANITARY
308MFR INSAN
New York District Office (NYK-DO)
4/28/2011
25QGT01MUSHROOM, COMMON (AGARICUS BISPORUS), PIECES AND STEMS, SLICED
2920PESTICIDES
New York District Office (NYK-DO)

Frequently Asked Questions

What is HIMALYA INTERNATIONAL LTD.'s FDA import refusal history?

HIMALYA INTERNATIONAL LTD. (FEI: 3004250068) has 3 FDA import refusal record(s) in our database, spanning from 4/28/2011 to 7/16/2015.

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. HIMALYA INTERNATIONAL LTD.'s FEI number is 3004250068.

What types of violations has HIMALYA INTERNATIONAL LTD. received?

HIMALYA INTERNATIONAL LTD. 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 HIMALYA INTERNATIONAL LTD. come from?

All FDA import refusal data for HIMALYA INTERNATIONAL LTD. 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.