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TDI ONLINE LTD

⚠️ Moderate Risk

FEI: 3014768031 • Watford • UNITED KINGDOM

FEI

FEI Number

3014768031

📍

Location

Watford

🇬🇧
🏢

Address

Unit 11, Olds Close, Watford, , United Kingdom

Moderate Risk

FDA Import Risk Assessment

43.0
LowModerateHighCritical

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

Statistics

6
Total Refusals
5
Unique Violations
12/8/2022
Latest Refusal
3/8/2019
Earliest Refusal

Score Breakdown

Violation Severity
68.2×40%
Refusal Volume
31.3×30%
Recency
23.7×20%
Frequency
16.0×10%
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

844×

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.

24803×

RXPERSONAL

The article appears to be a device which requires a prescription from your doctor.

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).

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.

Refusal History

DateProductViolationsDivision
12/8/2022
86LPLLENSES, SOFT CONTACT, DAILY WEAR
118NOT LISTED
3280FRNMFGREG
Division of Southeast Imports (DSEI)
3/15/2019
86LPMLENSES, SOFT CONTACT, EXTENDED WEAR
237NO PMA
84RX DEVICE
Division of Southeast Imports (DSEI)
3/15/2019
86LPMLENSES, SOFT CONTACT, EXTENDED WEAR
237NO PMA
Division of Southeast Imports (DSEI)
3/8/2019
86LPMLENSES, SOFT CONTACT, EXTENDED WEAR
2480RXPERSONAL
84RX DEVICE
Division of Southeast Imports (DSEI)
3/8/2019
86LPMLENSES, SOFT CONTACT, EXTENDED WEAR
2480RXPERSONAL
84RX DEVICE
Division of Southeast Imports (DSEI)
3/8/2019
86LPMLENSES, SOFT CONTACT, EXTENDED WEAR
2480RXPERSONAL
84RX DEVICE
Division of Southeast Imports (DSEI)

Frequently Asked Questions

What is TDI ONLINE LTD's FDA import refusal history?

TDI ONLINE LTD (FEI: 3014768031) has 6 FDA import refusal record(s) in our database, spanning from 3/8/2019 to 12/8/2022.

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. TDI ONLINE LTD's FEI number is 3014768031.

What types of violations has TDI ONLINE LTD received?

TDI ONLINE LTD 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 TDI ONLINE LTD come from?

All FDA import refusal data for TDI ONLINE 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.