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Peter's Delight Inc.

✅ Low Risk

FEI: 3008302522 • Saint George'S • GRENADA

FEI

FEI Number

3008302522

📍

Location

Saint George'S

🇬🇩

Country

GRENADA
🏢

Address

Golf Course, , Saint George'S, , Grenada

Low Risk

FDA Import Risk Assessment

23.3
LowModerateHighCritical

This firm has a minimal history of FDA import refusals with low-severity violations.

Statistics

2
Total Refusals
1
Unique Violations
7/1/2010
Latest Refusal
7/1/2010
Earliest Refusal

Score Breakdown

Violation Severity
40.0×40%
Refusal Volume
17.7×30%
Recency
0.0×20%
Frequency
20.0×10%
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

3282×

USUAL NAME

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)(1) of the FD&C Act in that the label fails to bear the common or usual name of the food, if any there be.

Refusal History

DateProductViolationsDivision
7/1/2010
21JHT14PLUM, JAM, JELLY, PRESERVES, MARMALADE, BUTTER OR CANDIED
328USUAL NAME
New York District Office (NYK-DO)
7/1/2010
21JHT14PLUM, JAM, JELLY, PRESERVES, MARMALADE, BUTTER OR CANDIED
328USUAL NAME
New York District Office (NYK-DO)

Frequently Asked Questions

What is Peter's Delight Inc.'s FDA import refusal history?

Peter's Delight Inc. (FEI: 3008302522) has 2 FDA import refusal record(s) in our database, spanning from 7/1/2010 to 7/1/2010.

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. Peter's Delight Inc.'s FEI number is 3008302522.

What types of violations has Peter's Delight Inc. received?

Peter's Delight Inc. has been cited for 1 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 Peter's Delight Inc. come from?

All FDA import refusal data for Peter's Delight Inc. 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.