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Nitinol Devices and Components Costa Rica, S.R.L.

⚠️ Moderate Risk

FEI: 3009018440 • El Coyol, Alajuela • COSTA RICA

FEI

FEI Number

3009018440

📍

Location

El Coyol, Alajuela

🇨🇷

Country

COSTA RICA
🏢

Address

Coyol Free Zone, Building 14, Building B14, B15, B25, El Coyol, Alajuela, Costa Rica

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
5/5/2017
Latest Refusal
5/5/2017
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
5/5/2017
95RFPREMOTE CONTROLLER, LASER, DATA MEASUREMENT, TRANSMIT
47NON STD
Division of Southeast Imports (DSEI)

Frequently Asked Questions

What is Nitinol Devices and Components Costa Rica, S.R.L.'s FDA import refusal history?

Nitinol Devices and Components Costa Rica, S.R.L. (FEI: 3009018440) has 1 FDA import refusal record(s) in our database, spanning from 5/5/2017 to 5/5/2017.

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. Nitinol Devices and Components Costa Rica, S.R.L.'s FEI number is 3009018440.

What types of violations has Nitinol Devices and Components Costa Rica, S.R.L. received?

Nitinol Devices and Components Costa Rica, S.R.L. 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 Nitinol Devices and Components Costa Rica, S.R.L. come from?

All FDA import refusal data for Nitinol Devices and Components Costa Rica, S.R.L. 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.