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LABORATORIES SANFER S.A. DE C.V.

⚠️ Moderate Risk

FEI: 3000328435 • Ciudad De Mexico, Ciudad de Mexico • MEXICO

FEI

FEI Number

3000328435

📍

Location

Ciudad De Mexico, Ciudad de Mexico

🇲🇽

Country

MEXICO
🏢

Address

Avenida Calzada De Tlalpan 550, Col. Moderna, Benito Juarez, Ciudad De Mexico, Ciudad de Mexico, Mexico

Moderate Risk

FDA Import Risk Assessment

41.4
LowModerateHighCritical

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

Statistics

2
Total Refusals
1
Unique Violations
4/14/2017
Latest Refusal
10/22/2002
Earliest Refusal

Score Breakdown

Violation Severity
90.0×40%
Refusal Volume
17.7×30%
Recency
0.0×20%
Frequency
1.4×10%
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

752×

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).

Refusal History

DateProductViolationsDivision
4/14/2017
66VCE99MISCELLANEOUS PATENT MEDICINES, ETC.
75UNAPPROVED
Division of Southeast Imports (DSEI)
10/22/2002
56BCZ03AMOXICILLIN TRIHYDRATE (PENICILLIN, SYNTHETICALLY PRODUCED)
75UNAPPROVED
Chicago District Office (CHI-DO)

Frequently Asked Questions

What is LABORATORIES SANFER S.A. DE C.V.'s FDA import refusal history?

LABORATORIES SANFER S.A. DE C.V. (FEI: 3000328435) has 2 FDA import refusal record(s) in our database, spanning from 10/22/2002 to 4/14/2017.

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. LABORATORIES SANFER S.A. DE C.V.'s FEI number is 3000328435.

What types of violations has LABORATORIES SANFER S.A. DE C.V. received?

LABORATORIES SANFER S.A. 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 LABORATORIES SANFER S.A. DE C.V. come from?

All FDA import refusal data for LABORATORIES SANFER S.A. 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.