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TRIVITA, INC.

⚠️ Moderate Risk

FEI: 3004320651 • Scottsdale, AZ • UNITED STATES

FEI

FEI Number

3004320651

📍

Location

Scottsdale, AZ

🇺🇸
🏢

Address

16100 N Greenway Hayden Loop Ste 950, , Scottsdale, AZ, United States

Moderate Risk

FDA Import Risk Assessment

38.3
LowModerateHighCritical

This firm has a moderate history of FDA import refusals. Some attention may be warranted.

Statistics

1
Total Refusals
2
Unique Violations
12/27/2012
Latest Refusal
12/27/2012
Earliest Refusal

Score Breakdown

Violation Severity
85.0×40%
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

751×

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).

831×

NO PROCESS

The article is subject to refusal of admission pursuant to Section 801(a)(3) in that the manufacturer's failure to file a scheduled process demonstrates that the product is not being manufactured under the mandatory provisions of 21 CFR Part 108 and therefore appears to have been manufactured, processed, or packed, under insanitary conditions whereby it may have been rendered injurious to health.

Refusal History

DateProductViolationsDivision
12/27/2012
54FCY99HERBALS & BOTANICALS (NOT TEAS), N.E.C.
75UNAPPROVED
83NO PROCESS
Los Angeles District Office (LOS-DO)

Frequently Asked Questions

What is TRIVITA, INC.'s FDA import refusal history?

TRIVITA, INC. (FEI: 3004320651) has 1 FDA import refusal record(s) in our database, spanning from 12/27/2012 to 12/27/2012.

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. TRIVITA, INC.'s FEI number is 3004320651.

What types of violations has TRIVITA, INC. received?

TRIVITA, INC. 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 TRIVITA, INC. come from?

All FDA import refusal data for TRIVITA, 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.