Grupo Manufacturero Rio Grande , S.A. De C.V.
✅ Low Risk
FEI: 1000481444 • Coah. • MEXICO
FEI Number
1000481444
Location
Coah.
Country
MEXICOAddress
Privada Aldama #113 col Las Fuentes, , Piedras Negras, Coah., , Mexico
Low Risk
FDA Import Risk Assessment
This firm has a minimal history of FDA import refusals with low-severity 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
NO ENGLISH
Required label or labeling appears to not be in English in violation of 21 C.F.R. 801.15(c)(1)
Refusal History
| Date | Product | Violations | Division |
|---|---|---|---|
| 12/12/2011 | 79GARSUTURE, NONABSORBABLE, SYNTHETIC, POLYAMIDE | 3260NO ENGLISH | Division of Southwest Imports (DSWI) |
| 12/12/2011 | 79GALSUTURE, ABSORBABLE, NATURAL | 3260NO ENGLISH | Division of Southwest Imports (DSWI) |
| 12/12/2011 | 79GALSUTURE, ABSORBABLE, NATURAL | 3260NO ENGLISH | Division of Southwest Imports (DSWI) |
| 12/12/2011 | 79GAMSUTURE, ABSORBABLE, SYNTHETIC, POLYGLYCOLIC ACID | 3260NO ENGLISH | Division of Southwest Imports (DSWI) |
Frequently Asked Questions
What is Grupo Manufacturero Rio Grande , S.A. De C.V.'s FDA import refusal history?
Grupo Manufacturero Rio Grande , S.A. De C.V. (FEI: 1000481444) has 4 FDA import refusal record(s) in our database, spanning from 12/12/2011 to 12/12/2011.
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. Grupo Manufacturero Rio Grande , S.A. De C.V.'s FEI number is 1000481444.
What types of violations has Grupo Manufacturero Rio Grande , S.A. De C.V. received?
Grupo Manufacturero Rio Grande , 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 Grupo Manufacturero Rio Grande , S.A. De C.V. come from?
All FDA import refusal data for Grupo Manufacturero Rio Grande , 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.