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AMBA DOCKSIDE TECHNOLOGY LIMITED

⚠️ Moderate Risk

FEI: 3015939218 • Waterlooville, Hampshire • UNITED KINGDOM

FEI

FEI Number

3015939218

📍

Location

Waterlooville, Hampshire

🇬🇧
🏢

Address

20 Aston Road, Unit, Waterlooville, Hampshire, United Kingdom

Moderate Risk

FDA Import Risk Assessment

32.3
LowModerateHighCritical

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

Statistics

1
Total Refusals
1
Unique Violations
11/21/2019
Latest Refusal
11/21/2019
Earliest Refusal

Score Breakdown

Violation Severity
70.0×40%
Refusal Volume
11.2×30%
Recency
0.0×20%
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

471×

NON STD

The article is subject to refusal of admission pursuant to section 536(a) of the Federal Food, Drug, and Cosmetic Act (FFDCA) in that it appears to be an electronic product offered for importation into the United States which fails to comply with an applicable standard prescribed pursuant to section 534 of the FFDCA.

Refusal History

DateProductViolationsDivision
11/21/2019
95RDWGENERAL PURPOSE LASER PRODUCTS, NON-MEDICAL
47NON STD
Division of Southeast Imports (DSEI)

Frequently Asked Questions

What is AMBA DOCKSIDE TECHNOLOGY LIMITED's FDA import refusal history?

AMBA DOCKSIDE TECHNOLOGY LIMITED (FEI: 3015939218) has 1 FDA import refusal record(s) in our database, spanning from 11/21/2019 to 11/21/2019.

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. AMBA DOCKSIDE TECHNOLOGY LIMITED's FEI number is 3015939218.

What types of violations has AMBA DOCKSIDE TECHNOLOGY LIMITED received?

AMBA DOCKSIDE TECHNOLOGY LIMITED has been cited for 1 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 AMBA DOCKSIDE TECHNOLOGY LIMITED come from?

All FDA import refusal data for AMBA DOCKSIDE TECHNOLOGY LIMITED 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.