NRG Group Limited
⚠️ High Risk
FEI: 3009927373 • Auckland, Auckland • NEW ZEALAND
FEI Number
3009927373
Location
Auckland, Auckland
Country
NEW ZEALANDAddress
Avondale, 438b Rosebank Road, Auckland, Auckland, New Zealand
High Risk
FDA Import Risk Assessment
This firm has a significant history of FDA import refusals with notable violations.
Statistics
Score Breakdown
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
UNAPPROVED
The article is subject to refusal of admission pursuant to Section 801(a)(3) in that it appears to be a new drug within the meaning of Section 201(p) without an approved New Drug Application (NDA).
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.
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.
DIETARYLBL
The article is subject to refusal of admission pursuant to Section 801(a)(3) of the FD&C Act in that it is a dietary supplement that appears to be misbranded within the meaning of Section 403(s)(2)(B) of the FD&C Act in that the label or labeling fails to identify the product by using the term "dietary supplement", which term may be modified with the name of such an ingredient.
Refusal History
| Date | Product | Violations | Division |
|---|---|---|---|
| 6/9/2025 | 41YYY99DIETARY CONVENTIONAL FOODS, N.E.C. | 75UNAPPROVED | Division of Southeast Imports (DSEI) |
| 6/9/2025 | 54FCY99HERBALS & BOTANICALS (NOT TEAS), N.E.C. | 75UNAPPROVED | Division of Southeast Imports (DSEI) |
| 7/11/2016 | 54ADY99VITAMIN, N.E.C. | Division of Southeast Imports (DSEI) | |
| 7/11/2016 | 54ADY99VITAMIN, N.E.C. | Division of Southeast Imports (DSEI) | |
| 6/30/2016 | 54YCY99VITAMIN, MINERAL, PROTEINS AND UNCONVENTIONAL DIETARY SPECIALITIES FOR HUMANS AND ANIMALS, N.E.C. | New Orleans District Office (NOL-DO) | |
| 6/30/2016 | 54YCY99VITAMIN, MINERAL, PROTEINS AND UNCONVENTIONAL DIETARY SPECIALITIES FOR HUMANS AND ANIMALS, N.E.C. | Division of Southeast Imports (DSEI) | |
| 6/10/2016 | 54ABA90MULTIPLE VITAMINS (MVI-12 VITAMIN COMBO) (VITAMIN) | New Orleans District Office (NOL-DO) | |
| 6/8/2016 | 54ABL99VITAMIN, N.E.C. | Division of Southeast Imports (DSEI) | |
| 6/8/2016 | 54ABL99VITAMIN, N.E.C. | Division of Southeast Imports (DSEI) | |
| 6/8/2016 | 54ABL99VITAMIN, N.E.C. | Division of Southeast Imports (DSEI) | |
| 6/8/2016 | 54ABL99VITAMIN, N.E.C. | Division of Southeast Imports (DSEI) | |
| 6/8/2016 | 54ABL99VITAMIN, N.E.C. | Division of Southeast Imports (DSEI) |
Frequently Asked Questions
What is NRG Group Limited's FDA import refusal history?
NRG Group Limited (FEI: 3009927373) has 12 FDA import refusal record(s) in our database, spanning from 6/8/2016 to 6/9/2025.
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. NRG Group Limited's FEI number is 3009927373.
What types of violations has NRG Group Limited received?
NRG Group Limited 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 NRG Group Limited come from?
All FDA import refusal data for NRG Group Limited 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.