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JANE HU

⚠️ Moderate Risk

FEI: 3016613219 • Zhejiang Provin • CHINA

FEI

FEI Number

3016613219

📍

Location

Zhejiang Provin

🇨🇳

Country

CHINA
🏢

Address

Room 1-507 No 1 Buildin, , Zhejiang Provin, , China

Moderate Risk

FDA Import Risk Assessment

25.1
LowModerateHighCritical

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

Statistics

1
Total Refusals
5
Unique Violations
6/5/2020
Latest Refusal
6/5/2020
Earliest Refusal

Score Breakdown

Violation Severity
52.0×40%
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

1181×

NOT LISTED

It appears the drug or device is not included in a list required by Section 510(j), or a notice or other information respecting it was not provided as required by section 510(j) or 510(k).

161×

DIRECTIONS

The article is subject to refusal of admission pursuant to section 801(a)(3) in that it is a device whose label appears to not bear adequate directions for use.

32801×

FRNMFGREG

The article is subject to refusal of admission pursuant to section 801(a)(3) in that it appears to be misbranded as defined in section 502(o) of the FD&C Act. It appears that it was manufactured, prepared, propagated, compounded, or processed in an establishment not duly registered under section 510 of the Act.

3331×

LACKS FIRM

The article is in package form and appears to not bear a label containing the name and place of business of the manufacturer, packer, or distributor.

5081×

NO 510(K)

The article is subject to refusal of admission pursuant to Section 801(a)(3) in that it is a post 1976 device for which a Section 510(k)application does not appear to have been determined substantially equivalent or otherwise filed.

Refusal History

DateProductViolationsDivision
6/5/2020
83QJRREAGENTS, 2019-NOVEL CORONAVIRUS NUCLEIC ACID
118NOT LISTED
16DIRECTIONS
3280FRNMFGREG
333LACKS FIRM
508NO 510(K)
Division of Southeast Imports (DSEI)

Frequently Asked Questions

What is JANE HU's FDA import refusal history?

JANE HU (FEI: 3016613219) has 1 FDA import refusal record(s) in our database, spanning from 6/5/2020 to 6/5/2020.

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. JANE HU's FEI number is 3016613219.

What types of violations has JANE HU received?

JANE HU 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 JANE HU come from?

All FDA import refusal data for JANE HU 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.