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FLEXTRONICS MANUFACTURING JUAREZ S. DE R.L. DE C.V.

⚠️ Moderate Risk

FEI: 3007344957 • Juarez, Chihuahua • MEXICO

FEI

FEI Number

3007344957

📍

Location

Juarez, Chihuahua

🇲🇽

Country

MEXICO
🏢

Address

Boulevard Independencia NO. 4240, Col. PAPALOTE, Juarez, Chihuahua, Mexico

Moderate Risk

FDA Import Risk Assessment

49.0
LowModerateHighCritical

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

Statistics

7
Total Refusals
1
Unique Violations
5/31/2016
Latest Refusal
5/11/2016
Earliest Refusal

Score Breakdown

Violation Severity
80.0×40%
Refusal Volume
33.5×30%
Recency
0.0×20%
Frequency
70.0×10%
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

2377×

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).

Refusal History

DateProductViolationsDivision
5/31/2016
80FMINEEDLE, HYPODERMIC, SINGLE LUMEN
237NO PMA
Southwest Import District Office (SWI-DO)
5/31/2016
80FMINEEDLE, HYPODERMIC, SINGLE LUMEN
237NO PMA
Southwest Import District Office (SWI-DO)
5/31/2016
80FMINEEDLE, HYPODERMIC, SINGLE LUMEN
237NO PMA
Southwest Import District Office (SWI-DO)
5/31/2016
80FMINEEDLE, HYPODERMIC, SINGLE LUMEN
237NO PMA
Southwest Import District Office (SWI-DO)
5/11/2016
80FMINEEDLE, HYPODERMIC, SINGLE LUMEN
237NO PMA
Southwest Import District Office (SWI-DO)
5/11/2016
80FMINEEDLE, HYPODERMIC, SINGLE LUMEN
237NO PMA
Southwest Import District Office (SWI-DO)
5/11/2016
80FMINEEDLE, HYPODERMIC, SINGLE LUMEN
237NO PMA
Southwest Import District Office (SWI-DO)

Frequently Asked Questions

What is FLEXTRONICS MANUFACTURING JUAREZ S. DE R.L. DE C.V.'s FDA import refusal history?

FLEXTRONICS MANUFACTURING JUAREZ S. DE R.L. DE C.V. (FEI: 3007344957) has 7 FDA import refusal record(s) in our database, spanning from 5/11/2016 to 5/31/2016.

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. FLEXTRONICS MANUFACTURING JUAREZ S. DE R.L. DE C.V.'s FEI number is 3007344957.

What types of violations has FLEXTRONICS MANUFACTURING JUAREZ S. DE R.L. DE C.V. received?

FLEXTRONICS MANUFACTURING JUAREZ S. DE R.L. DE C.V. 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 FLEXTRONICS MANUFACTURING JUAREZ S. DE R.L. DE C.V. come from?

All FDA import refusal data for FLEXTRONICS MANUFACTURING JUAREZ S. DE R.L. DE C.V. 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.