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The Immortalitea Company

✅ Low Risk

FEI: 3004802110 • Grandville, MI • UNITED STATES

FEI

FEI Number

3004802110

📍

Location

Grandville, MI

🇺🇸
🏢

Address

2885 Sanford Ave SW Unit 26299, , Grandville, MI, United States

Low Risk

FDA Import Risk Assessment

22.3
LowModerateHighCritical

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

Statistics

1
Total Refusals
2
Unique Violations
7/27/2017
Latest Refusal
7/27/2017
Earliest Refusal

Score Breakdown

Violation Severity
45.0×40%
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

2601×

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.

4821×

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
7/27/2017
54FBH99HERBALS & BOTANICALS (NOT TEAS), N.E.C.
260FALSE
482NUTRIT LBL
Division of Southeast Imports (DSEI)

Frequently Asked Questions

What is The Immortalitea Company's FDA import refusal history?

The Immortalitea Company (FEI: 3004802110) has 1 FDA import refusal record(s) in our database, spanning from 7/27/2017 to 7/27/2017.

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. The Immortalitea Company's FEI number is 3004802110.

What types of violations has The Immortalitea Company received?

The Immortalitea Company has been cited for 2 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 The Immortalitea Company come from?

All FDA import refusal data for The Immortalitea 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.