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Sythetek Industries Pty Ltd

⚠️ Moderate Risk

FEI: 3006445742 • Highett, Victoria • AUSTRALIA

FEI

FEI Number

3006445742

📍

Location

Highett, Victoria

🇦🇺

Country

AUSTRALIA
🏢

Address

U 1 539 Highett Rd, , Highett, Victoria, Australia

Moderate Risk

FDA Import Risk Assessment

35.3
LowModerateHighCritical

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

Statistics

2
Total Refusals
4
Unique Violations
12/3/2007
Latest Refusal
11/29/2007
Earliest Refusal

Score Breakdown

Violation Severity
70.0×40%
Refusal Volume
17.7×30%
Recency
0.0×20%
Frequency
20.0×10%
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).

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.

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).

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
12/3/2007
80FMFSYRINGE, PISTON
118NOT LISTED
508NO 510(K)
84RX DEVICE
New Orleans District Office (NOL-DO)
11/29/2007
54ACL05VITAMIN B12 (CYANOCOBALAMIN)
75UNAPPROVED
New Orleans District Office (NOL-DO)

Frequently Asked Questions

What is Sythetek Industries Pty Ltd's FDA import refusal history?

Sythetek Industries Pty Ltd (FEI: 3006445742) has 2 FDA import refusal record(s) in our database, spanning from 11/29/2007 to 12/3/2007.

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. Sythetek Industries Pty Ltd's FEI number is 3006445742.

What types of violations has Sythetek Industries Pty Ltd received?

Sythetek Industries Pty Ltd has been cited for 4 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 Sythetek Industries Pty Ltd come from?

All FDA import refusal data for Sythetek Industries Pty 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.