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Nuliv Biomedicine Inc

⚠️ Moderate Risk

FEI: 3010164010 • Pudong • CHINA

FEI

FEI Number

3010164010

📍

Location

Pudong

🇨🇳

Country

CHINA
🏢

Address

Room 6402 No 338 Jialilue Rd Zhangjiang, , Pudong, , China

Moderate Risk

FDA Import Risk Assessment

40.3
LowModerateHighCritical

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

Statistics

1
Total Refusals
1
Unique Violations
9/26/2013
Latest Refusal
9/26/2013
Earliest Refusal

Score Breakdown

Violation Severity
90.0×40%
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

37211×

PESTICIDE2

The article is subject to refusal of admission pursuant to section 801(a)(3) in that it appears to be adulterated because it contains a pesticide chemical, which is in violation of section 402(a)(2)(B). Contains:

Refusal History

DateProductViolationsDivision
9/26/2013
54FBR12GINSENG (HERBAL & BOTANICALS, NOT TEAS)
3721PESTICIDE2
Los Angeles District Office (LOS-DO)

Frequently Asked Questions

What is Nuliv Biomedicine Inc's FDA import refusal history?

Nuliv Biomedicine Inc (FEI: 3010164010) has 1 FDA import refusal record(s) in our database, spanning from 9/26/2013 to 9/26/2013.

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. Nuliv Biomedicine Inc's FEI number is 3010164010.

What types of violations has Nuliv Biomedicine Inc received?

Nuliv Biomedicine Inc 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 Nuliv Biomedicine Inc come from?

All FDA import refusal data for Nuliv Biomedicine 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.