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Premium Foods

⚠️ Moderate Risk

FEI: 3003952616 • Mumbai, Maharashtra • INDIA

FEI

FEI Number

3003952616

📍

Location

Mumbai, Maharashtra

🇮🇳

Country

INDIA
🏢

Address

N - 14 Altamount Road, , Mumbai, Maharashtra, India

Moderate Risk

FDA Import Risk Assessment

34.4
LowModerateHighCritical

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

Statistics

7
Total Refusals
6
Unique Violations
2/20/2004
Latest Refusal
12/16/2003
Earliest Refusal

Score Breakdown

Violation Severity
43.3×40%
Refusal Volume
33.5×30%
Recency
0.0×20%
Frequency
70.0×10%
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

2187×

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.

2765×

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.

3244×

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)).

113×

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).

2563×

INCONSPICU

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)).

4732×

LABELING

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

Refusal History

DateProductViolationsDivision
2/20/2004
03JFT07MIXED FILLED/ICED COOKIES,BISCUITS AND WAFERS
218LIST INGRE
276PRESRV LBL
San Francisco District Office (SAN-DO)
2/20/2004
03JFT07MIXED FILLED/ICED COOKIES,BISCUITS AND WAFERS
218LIST INGRE
San Francisco District Office (SAN-DO)
2/20/2004
03AFT03BISCUITS
218LIST INGRE
San Francisco District Office (SAN-DO)
12/16/2003
03HGY99PLAIN COOKIES,BISCUITS AND WAFERS, N.E.C.
218LIST INGRE
256INCONSPICU
276PRESRV LBL
324NO ENGLISH
473LABELING
Southwest Import District Office (SWI-DO)
12/16/2003
03JGY10CREME FILLED/ICED COOKIE,BISCUIT,WAFER
11UNSAFE COL
218LIST INGRE
276PRESRV LBL
324NO ENGLISH
Southwest Import District Office (SWI-DO)
12/16/2003
03HGY99PLAIN COOKIES,BISCUITS AND WAFERS, N.E.C.
11UNSAFE COL
218LIST INGRE
256INCONSPICU
276PRESRV LBL
324NO ENGLISH
473LABELING
Southwest Import District Office (SWI-DO)
12/16/2003
03JGY09FRUIT/FRUIT FLAVORED FILLED/ICED COOKIES,BISCUITS AND WAFERS
11UNSAFE COL
218LIST INGRE
256INCONSPICU
276PRESRV LBL
324NO ENGLISH
Southwest Import District Office (SWI-DO)

Frequently Asked Questions

What is Premium Foods's FDA import refusal history?

Premium Foods (FEI: 3003952616) has 7 FDA import refusal record(s) in our database, spanning from 12/16/2003 to 2/20/2004.

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. Premium Foods's FEI number is 3003952616.

What types of violations has Premium Foods received?

Premium Foods has been cited for 6 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 Premium Foods come from?

All FDA import refusal data for Premium Foods 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.