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ANHUI TIANKANG MEDICAL PRODUCTS CO., LTD.

⚠️ Moderate Risk

FEI: 3007590959 • Tianchang, Anhui • CHINA

FEI

FEI Number

3007590959

📍

Location

Tianchang, Anhui

🇨🇳

Country

CHINA
🏢

Address

No. 228 Weiyi Road, Economic Development Zone, Tianchang, Anhui, China

Moderate Risk

FDA Import Risk Assessment

40.5
LowModerateHighCritical

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

Statistics

2
Total Refusals
6
Unique Violations
5/23/2025
Latest Refusal
9/10/2015
Earliest Refusal

Score Breakdown

Violation Severity
51.4×40%
Refusal Volume
17.7×30%
Recency
72.3×20%
Frequency
2.1×10%
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

32802×

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.

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.

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.

4841×

DV NAME

The article appears to be a device and its labeling fails to bear the proprietary or established name.

841×

RX DEVICE

The article is subject to refusal of admission pursuant to Section 801(a)(3) in that it is a prescription device that appears to not feature a prescription device legend as required by 21 CFR 801.109.

Refusal History

DateProductViolationsDivision
5/23/2025
80MEGSYRINGE, ANTISTICK
3280FRNMFGREG
Division of West Coast Imports (DWCI)
9/10/2015
78GBMCATHETER, URETHRAL
118NOT LISTED
16DIRECTIONS
3280FRNMFGREG
333LACKS FIRM
484DV NAME
84RX DEVICE
Seattle District Office (SEA-DO)

Frequently Asked Questions

What is ANHUI TIANKANG MEDICAL PRODUCTS CO., LTD.'s FDA import refusal history?

ANHUI TIANKANG MEDICAL PRODUCTS CO., LTD. (FEI: 3007590959) has 2 FDA import refusal record(s) in our database, spanning from 9/10/2015 to 5/23/2025.

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. ANHUI TIANKANG MEDICAL PRODUCTS CO., LTD.'s FEI number is 3007590959.

What types of violations has ANHUI TIANKANG MEDICAL PRODUCTS CO., LTD. received?

ANHUI TIANKANG MEDICAL PRODUCTS CO., LTD. has been cited for 6 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 ANHUI TIANKANG MEDICAL PRODUCTS CO., LTD. come from?

All FDA import refusal data for ANHUI TIANKANG MEDICAL PRODUCTS 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.