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Bod-e Pro

⚠️ Moderate Risk

FEI: 3013395721 • Scottsdale, AZ • UNITED STATES

FEI

FEI Number

3013395721

📍

Location

Scottsdale, AZ

🇺🇸
🏢

Address

8132 N 87th Pl, , Scottsdale, AZ, United States

Moderate Risk

FDA Import Risk Assessment

43.8
LowModerateHighCritical

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

Statistics

4
Total Refusals
1
Unique Violations
6/25/2013
Latest Refusal
6/25/2013
Earliest Refusal

Score Breakdown

Violation Severity
80.0×40%
Refusal Volume
25.9×30%
Recency
0.0×20%
Frequency
40.0×10%
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

834×

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
6/25/2013
54YER99VITAMIN, MINERAL, PROTEINS AND UNCONVENTIONAL DIETARY SPECIALITIES FOR HUMANS AND ANIMALS, N.E.C.
83NO PROCESS
New York District Office (NYK-DO)
6/25/2013
54YER99VITAMIN, MINERAL, PROTEINS AND UNCONVENTIONAL DIETARY SPECIALITIES FOR HUMANS AND ANIMALS, N.E.C.
83NO PROCESS
New York District Office (NYK-DO)
6/25/2013
21VET15MANGOSTEEN, JUICE, MILK, CREME, DRINK OR NECTAR, SUB/TROPICAL FRUIT
83NO PROCESS
New York District Office (NYK-DO)
6/25/2013
21VHT15MANGOSTEEN, JUICE, MILK, CREME, DRINK OR NECTAR, SUB/TROPICAL FRUIT
83NO PROCESS
New York District Office (NYK-DO)

Frequently Asked Questions

What is Bod-e Pro's FDA import refusal history?

Bod-e Pro (FEI: 3013395721) has 4 FDA import refusal record(s) in our database, spanning from 6/25/2013 to 6/25/2013.

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. Bod-e Pro's FEI number is 3013395721.

What types of violations has Bod-e Pro received?

Bod-e Pro 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 Bod-e Pro come from?

All FDA import refusal data for Bod-e Pro 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.