Laboratorios Grim, S.A. de C.V.
⚠️ High Risk
FEI: 3005641358 • Mexico City • MEXICO
FEI Number
3005641358
Location
Mexico City
Country
MEXICOAddress
Rodriguez Saro No. 630, Col. Del Valle, Mexico City, , Mexico
High Risk
FDA Import Risk Assessment
This firm has a significant history of FDA import refusals with notable violations.
Statistics
Score Breakdown
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
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).
NOT LISTED
It appears the drug or device is not included in a list required by Section 510(j), or a notice or other information respecting it was not provided as required by section 510(j) or 510(k).
Refusal History
| Date | Product | Violations | Division |
|---|---|---|---|
| 4/18/2025 | 64EDY11CHYMOTRYPSIN (ENZYME) | Division of Southeast Imports (DSEI) | |
| 12/19/2021 | 56ECY20DOXYCYCLINE (TETRACYCLINES) | 75UNAPPROVED | Division of Southeast Imports (DSEI) |
| 6/24/2019 | 62GDK94KETOROLAC TROMETHAMINE (ANTI-INFLAMMATORY) | 75UNAPPROVED | Division of Southeast Imports (DSEI) |
Frequently Asked Questions
What is Laboratorios Grim, S.A. de C.V.'s FDA import refusal history?
Laboratorios Grim, S.A. de C.V. (FEI: 3005641358) has 3 FDA import refusal record(s) in our database, spanning from 6/24/2019 to 4/18/2025.
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. Laboratorios Grim, S.A. de C.V.'s FEI number is 3005641358.
What types of violations has Laboratorios Grim, S.A. de C.V. received?
Laboratorios Grim, S.A. de C.V. 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 Laboratorios Grim, S.A. de C.V. come from?
All FDA import refusal data for Laboratorios Grim, 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.