Pachranga International (P) Ltd
⚠️ Moderate Risk
FEI: 3004096719 • Panipat, Haryana • INDIA
FEI Number
3004096719
Location
Panipat, Haryana
Country
INDIAAddress
45, Huda, Industrial Area, Sector 25, Phase II, Panipat, Haryana, India
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
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.
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.
NO ENGLISH
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(f) of the FD&C Act in that any word, statement, or other information required by or under the authority of the FD&C Act to appear on the label or labeling is not prominently placed thereon with such conspicuousness (as compared with other words, statements, designs, or devices, in the labeling) and in such terms as to render it likely to be read and understood by the ordinary individual under customary terms of purchase and use (for example, label contains information in two or more languages but fails to repeat all required information in both languages in accordance with 21 CFR 101.15(c)(2), or label fails to include all required information in English in accordance with 21 CFR 101.15(c)(1), except in the case of articles distributed solely in the Commonwealth of Puerto Rico or in a Territory where the predominant language is one other than English)).
COLOR LBLG
The article appears to contain an artificial coloring and it fails to bear labeling stating that fact.
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:
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.
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).
UNSAFE COL
The article appears to be a color additive for the purposes of coloring only in or on drugs or devices, and is unsafe within the meaning of Section 721(a).
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.
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).
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).
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.
Refusal History
| Date | Product | Violations | Division |
|---|---|---|---|
| 10/14/2021 | 25ECP99MIXED VEGETABLES, N.E.C. | 83NO PROCESS | Division of Southwest Imports (DSWI) |
| 4/8/2011 | 21SET05MANGO (SUBTROPICAL AND TROPICAL FRUIT) | New York District Office (NYK-DO) | |
| 1/9/2007 | 25EEE99MIXED VEGETABLES, N.E.C. | Los Angeles District Office (LOS-DO) | |
| 6/27/2006 | 25EEP99MIXED VEGETABLES, N.E.C. | San Francisco District Office (SAN-DO) | |
| 6/27/2006 | 25EEP99MIXED VEGETABLES, N.E.C. | San Francisco District Office (SAN-DO) | |
| 3/23/2006 | 62UBL99ANTI-TUSSIVE/COLD N.E.C. | San Francisco District Office (SAN-DO) | |
| 3/23/2006 | 33EGY99HARD CANDY WITHOUT NUTS AND FRUIT, N.E.C. (WITHOUT CHOCOLATE) | San Francisco District Office (SAN-DO) | |
| 2/17/2006 | 25ECP99MIXED VEGETABLES, N.E.C. | 83NO PROCESS | San Francisco District Office (SAN-DO) |
| 9/8/2005 | 24TEP10CAULIFLOWER (LEAF & STEM VEGETABLE) | San Francisco District Office (SAN-DO) |
Frequently Asked Questions
What is Pachranga International (P) Ltd's FDA import refusal history?
Pachranga International (P) Ltd (FEI: 3004096719) has 9 FDA import refusal record(s) in our database, spanning from 9/8/2005 to 10/14/2021.
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. Pachranga International (P) Ltd's FEI number is 3004096719.
What types of violations has Pachranga International (P) Ltd received?
Pachranga International (P) Ltd 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 Pachranga International (P) Ltd come from?
All FDA import refusal data for Pachranga International (P) 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.