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Niagara Bottling

✅ Low Risk

FEI: 3015856477 • Diamond Bar, CA • UNITED STATES

FEI

FEI Number

3015856477

📍

Location

Diamond Bar, CA

🇺🇸
🏢

Address

1440 Bridgegate Dr, , Diamond Bar, CA, United States

Low Risk

FDA Import Risk Assessment

16.3
LowModerateHighCritical

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

Statistics

1
Total Refusals
1
Unique Violations
5/20/2021
Latest Refusal
5/20/2021
Earliest Refusal

Score Breakdown

Violation Severity
30.0×40%
Refusal Volume
11.2×30%
Recency
0.0×20%
Frequency
10.0×10%
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

3211×

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.

Refusal History

DateProductViolationsDivision
5/20/2021
29RGT01BOTTLED SPRING WATER, NONCARBONATED (NONMEDICINAL)
321LACKS N/C
Division of Northern Border Imports (DNBI)

Frequently Asked Questions

What is Niagara Bottling's FDA import refusal history?

Niagara Bottling (FEI: 3015856477) has 1 FDA import refusal record(s) in our database, spanning from 5/20/2021 to 5/20/2021.

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. Niagara Bottling's FEI number is 3015856477.

What types of violations has Niagara Bottling received?

Niagara Bottling 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 Niagara Bottling come from?

All FDA import refusal data for Niagara Bottling 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.