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SHENZHEN BIOTECHNOLOGY CO LTD

⚠️ Moderate Risk

FEI: 3032499999 • Shenzhen, Guangdong • CHINA

FEI

FEI Number

3032499999

📍

Location

Shenzhen, Guangdong

🇨🇳

Country

CHINA
🏢

Address

No 107 Fuwei Road Baoan, , Shenzhen, Guangdong, China

Moderate Risk

FDA Import Risk Assessment

42.5
LowModerateHighCritical

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

Statistics

1
Total Refusals
8
Unique Violations
12/9/2024
Latest Refusal
12/9/2024
Earliest Refusal

Score Breakdown

Violation Severity
56.3×40%
Refusal Volume
11.2×30%
Recency
78.3×20%
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).

22801×

DIRSEXMPT

The article is subject to refusal of admission pursuant to Section 801(a)(3) in that it appears to be a drug within the meaning of Section 201(g) and it lacks 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.

3361×

INCONSPICU

Information required by the Act to be on the label or labeling does not appear to be conspicuous enough as to render it likely to be read and understood by the ordinary individual under customary conditions of purchase and use.

3441×

WARNINGS

It appears to lack adequate warning against use in a pathological condition or by children where it may be dangerous to health or against an unsafe dose, method, administering duration, application, in manner/form, to protect users.

4831×

DRUG NAME

The article appears to be a drug and fails to bear the proprietary or established name and/or name and quantity of each active ingredient.

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).

Refusal History

DateProductViolationsDivision
12/9/2024
66YDK99EXHIBITS - OTHER DRUG RELATED ITEMS N.E.C.
118NOT LISTED
2280DIRSEXMPT
3280FRNMFGREG
333LACKS FIRM
336INCONSPICU
344WARNINGS
483DRUG NAME
75UNAPPROVED
Division of Southeast Imports (DSEI)

Frequently Asked Questions

What is SHENZHEN BIOTECHNOLOGY CO LTD's FDA import refusal history?

SHENZHEN BIOTECHNOLOGY CO LTD (FEI: 3032499999) has 1 FDA import refusal record(s) in our database, spanning from 12/9/2024 to 12/9/2024.

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. SHENZHEN BIOTECHNOLOGY CO LTD's FEI number is 3032499999.

What types of violations has SHENZHEN BIOTECHNOLOGY CO LTD received?

SHENZHEN BIOTECHNOLOGY CO LTD has been cited for 8 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 SHENZHEN BIOTECHNOLOGY CO LTD come from?

All FDA import refusal data for SHENZHEN BIOTECHNOLOGY CO LTD 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.