LABORATORIES GRIN SA DE CV
⚠️ Moderate Risk
FEI: 3013232782 • Ciudad De Mexico, Ciudad de Mexico • MEXICO
FEI Number
3013232782
Location
Ciudad De Mexico, Ciudad de Mexico
Country
MEXICOAddress
Calle Rodriguez Saro Ben 630, Col. Del Valle Sur, Benito Juarez, Ciudad De Mexico, Ciudad de Mexico, Mexico
Moderate Risk
FDA Import Risk Assessment
This firm has a moderate history of FDA import refusals. Some attention may be warranted.
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
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).
NO 510(K)
The article is subject to refusal of admission pursuant to Section 801(a)(3) in that it is a post 1976 device for which a Section 510(k)application does not appear to have been determined substantially equivalent or otherwise filed.
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
Frequently Asked Questions
What is LABORATORIES GRIN SA DE CV's FDA import refusal history?
LABORATORIES GRIN SA DE CV (FEI: 3013232782) has 2 FDA import refusal record(s) in our database, spanning from 12/23/2016 to 6/15/2023.
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 GRIN SA DE CV's FEI number is 3013232782.
What types of violations has LABORATORIES GRIN SA DE CV received?
LABORATORIES GRIN SA DE CV has been cited for 3 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 GRIN SA DE CV come from?
All FDA import refusal data for LABORATORIES GRIN SA DE CV 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.