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English Provender Company

⚠️ Moderate Risk

FEI: 3009653397 • Newbury, Berkshire • UNITED KINGDOM

FEI

FEI Number

3009653397

📍

Location

Newbury, Berkshire

🇬🇧
🏢

Address

Buckner Croke Way, , Newbury, Berkshire, United Kingdom

Moderate Risk

FDA Import Risk Assessment

38.8
LowModerateHighCritical

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

Statistics

8
Total Refusals
4
Unique Violations
7/10/2006
Latest Refusal
1/29/2003
Earliest Refusal

Score Breakdown

Violation Severity
64.7×40%
Refusal Volume
35.3×30%
Recency
0.0×20%
Frequency
23.2×10%
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

837×

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.

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.

623×

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).

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.

Refusal History

DateProductViolationsDivision
7/10/2006
25NCI11SHALLOT, WITH SAUCE
321LACKS N/C
482NUTRIT LBL
83NO PROCESS
New York District Office (NYK-DO)
7/10/2006
28BCI11GARLIC, GROUND, CRACKED (SPICE)
321LACKS N/C
482NUTRIT LBL
New York District Office (NYK-DO)
7/10/2006
25JCI24GINGER ROOT (ROOT & TUBER VEGETABLE)
321LACKS N/C
62NEEDS FCE
83NO PROCESS
New York District Office (NYK-DO)
12/5/2005
25JCE21GARLIC BULB (ROOT & TUBER VEGETABLE)
83NO PROCESS
Baltimore District Office (BLT-DO)
10/12/2005
25JCE21GARLIC BULB (ROOT & TUBER VEGETABLE)
83NO PROCESS
San Francisco District Office (SAN-DO)
7/27/2005
25JCE02HORSERADISH (ROOT & TUBER VEGETABLE)
83NO PROCESS
Baltimore District Office (BLT-DO)
1/29/2003
37JCE99SAUCES, N.E.C.
62NEEDS FCE
83NO PROCESS
New York District Office (NYK-DO)
1/29/2003
25NCE25ONION BULB (YELLOW, WHITE, RED, ETC.), WITH SAUCE
62NEEDS FCE
83NO PROCESS
New York District Office (NYK-DO)

Frequently Asked Questions

What is English Provender Company's FDA import refusal history?

English Provender Company (FEI: 3009653397) has 8 FDA import refusal record(s) in our database, spanning from 1/29/2003 to 7/10/2006.

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. English Provender Company's FEI number is 3009653397.

What types of violations has English Provender Company received?

English Provender Company has been cited for 4 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 English Provender Company come from?

All FDA import refusal data for English Provender Company 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.