ImportRefusal LogoImportRefusal

TERAPIA CELULAR RG

⚠️ Moderate Risk

FEI: 3038560417 • Mexico City • MEXICO

FEI

FEI Number

3038560417

📍

Location

Mexico City

🇲🇽

Country

MEXICO
🏢

Address

Venustiano Carran 15220, , Mexico City, , Mexico

Moderate Risk

FDA Import Risk Assessment

46.7
LowModerateHighCritical

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

Statistics

1
Total Refusals
2
Unique Violations
8/15/2025
Latest Refusal
8/15/2025
Earliest Refusal

Score Breakdown

Violation Severity
60.0×40%
Refusal Volume
11.2×30%
Recency
91.7×20%
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

32601×

NO ENGLISH

Required label or labeling appears to not be in English in violation of 21 C.F.R. 801.15(c)(1)

751×

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
8/15/2025
54YBR99VITAMIN, MINERAL, PROTEINS AND UNCONVENTIONAL DIETARY SPECIALITIES FOR HUMANS AND ANIMALS, N.E.C.
3260NO ENGLISH
75UNAPPROVED
Division of Southeast Imports (DSEI)

Frequently Asked Questions

What is TERAPIA CELULAR RG's FDA import refusal history?

TERAPIA CELULAR RG (FEI: 3038560417) has 1 FDA import refusal record(s) in our database, spanning from 8/15/2025 to 8/15/2025.

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. TERAPIA CELULAR RG's FEI number is 3038560417.

What types of violations has TERAPIA CELULAR RG received?

TERAPIA CELULAR RG has been cited for 2 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 TERAPIA CELULAR RG come from?

All FDA import refusal data for TERAPIA CELULAR RG 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.