Naturalife Eco Vite Laboratories dba Paragon Laboratories
⚠️ Moderate Risk
FEI: 1000518758 • Torrance, CA • UNITED STATES
FEI Number
1000518758
Location
Torrance, CA
Country
UNITED STATESAddress
20433 Earl St, , Torrance, CA, United States
Moderate Risk
FDA Import Risk Assessment
This firm has a moderate history of FDA import refusals. Some attention may be warranted.
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
POISONOUS
The article is subject to refusal of admission pursuant to Section 801(a)(3) in that it appears to bear or contain a poisonous or deleterious substance which may render the article injurious to health. Contains:
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.
NCONTACT
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(y) of the FD&C Act in that the dietary supplement label fails to bear a domestic address or phone number through which the responsible person (as described in section 761 of the FD&C Act) may receive a report of a serious adverse event with such dietary supplement.
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.
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).
Refusal History
| Date | Product | Violations | Division |
|---|---|---|---|
| 8/13/2019 | 54ACR90MULTIPLE VITAMINS (MVI-12 VITAMIN COMBO) (VITAMIN) | Division of West Coast Imports (DWCI) | |
| 8/13/2019 | 54FCL99HERBALS & BOTANICALS (NOT TEAS), N.E.C. | Division of West Coast Imports (DWCI) | |
| 8/3/2011 | 54YCY99VITAMIN, MINERAL, PROTEINS AND UNCONVENTIONAL DIETARY SPECIALITIES FOR HUMANS AND ANIMALS, N.E.C. | 75UNAPPROVED | Cincinnati District Office (CIN-DO) |
| 5/7/2009 | 54CCZ05L-CYSTEINE (PROTEIN) | 251POISONOUS | Los Angeles District Office (LOS-DO) |
Frequently Asked Questions
What is Naturalife Eco Vite Laboratories dba Paragon Laboratories's FDA import refusal history?
Naturalife Eco Vite Laboratories dba Paragon Laboratories (FEI: 1000518758) has 4 FDA import refusal record(s) in our database, spanning from 5/7/2009 to 8/13/2019.
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. Naturalife Eco Vite Laboratories dba Paragon Laboratories's FEI number is 1000518758.
What types of violations has Naturalife Eco Vite Laboratories dba Paragon Laboratories received?
Naturalife Eco Vite Laboratories dba Paragon Laboratories has been cited for 5 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 Naturalife Eco Vite Laboratories dba Paragon Laboratories come from?
All FDA import refusal data for Naturalife Eco Vite Laboratories dba Paragon Laboratories 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.