ImportRefusal LogoImportRefusal

SURE BIO TECH

⚠️ Moderate Risk

FEI: 3016749399 • Qingdao City Shandong, Shandong • CHINA

FEI

FEI Number

3016749399

📍

Location

Qingdao City Shandong, Shandong

🇨🇳

Country

CHINA
🏢

Address

No.369 Hedong Road, Hi-Tech Industrial Development, , Qingdao City Shandong, Shandong, China

Moderate Risk

FDA Import Risk Assessment

38.9
LowModerateHighCritical

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

Statistics

3
Total Refusals
5
Unique Violations
4/6/2022
Latest Refusal
4/1/2021
Earliest Refusal

Score Breakdown

Violation Severity
68.3×40%
Refusal Volume
22.3×30%
Recency
9.6×20%
Frequency
29.6×10%
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

2372×

NO PMA

The article is subject to refusal of admission pursuant to Section 801(a)(3) in that the device appears to be a Class III device and does not appear to have in effect an approved application for premarket approval pursuant to Section 515 of the Act, or an exemption pursuant to Section 520(g)(1).

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).

23801×

NO PMA/PDP

The article appears to be a class III dev.w/o an approved applic. for premarket approval, and/or a notice of completion of product development protocol filed per section 515(b) or exempt per sect.520(g)(1).

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.

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
4/6/2022
83QKOREAGENT, CORONAVIRUS SEROLOGICAL
2380NO PMA/PDP
Division of Southeast Imports (DSEI)
4/6/2022
83QKOREAGENT, CORONAVIRUS SEROLOGICAL
237NO PMA
Division of Southeast Imports (DSEI)
4/1/2021
83QKOREAGENT, CORONAVIRUS SEROLOGICAL
118NOT LISTED
237NO PMA
3280FRNMFGREG
508NO 510(K)
Division of Southeast Imports (DSEI)

Frequently Asked Questions

What is SURE BIO TECH's FDA import refusal history?

SURE BIO TECH (FEI: 3016749399) has 3 FDA import refusal record(s) in our database, spanning from 4/1/2021 to 4/6/2022.

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. SURE BIO TECH's FEI number is 3016749399.

What types of violations has SURE BIO TECH received?

SURE BIO TECH 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 SURE BIO TECH come from?

All FDA import refusal data for SURE BIO TECH 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.