ImportRefusal LogoImportRefusal

Baxter Corporation

⚠️ Moderate Risk

FEI: 3000251214 • Mississauga, ON • CANADA

FEI

FEI Number

3000251214

📍

Location

Mississauga, ON

🇨🇦

Country

CANADA
🏢

Address

4 Robert Speck Parkway Ste 700, , Mississauga, ON, Canada

Moderate Risk

FDA Import Risk Assessment

28.3
LowModerateHighCritical

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

Statistics

1
Total Refusals
3
Unique Violations
10/23/2020
Latest Refusal
10/23/2020
Earliest Refusal

Score Breakdown

Violation Severity
60.0×40%
Refusal Volume
11.2×30%
Recency
0.0×20%
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

1181×

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).

271×

DRUG GMPS

The article is subject to refusal of admission pursuant to Section 801(a)(3) in that the methods used in and controls used for the manufacture, processing, packing, or holding of drugs and other products do not appear to conform to current good manufacturing practices within the meaning of Section 501(a)(2)(B).

32801×

FRNMFGREG

The article is subject to refusal of admission pursuant to section 801(a)(3) in that it appears to be misbranded as defined in section 502(o) of the FD&C Act. It appears that it was manufactured, prepared, propagated, compounded, or processed in an establishment not duly registered under section 510 of the Act.

Refusal History

DateProductViolationsDivision
10/23/2020
65RDK19SODIUM CHLORIDE (REPLENISHER)
118NOT LISTED
27DRUG GMPS
3280FRNMFGREG
Division of Northern Border Imports (DNBI)

Frequently Asked Questions

What is Baxter Corporation's FDA import refusal history?

Baxter Corporation (FEI: 3000251214) has 1 FDA import refusal record(s) in our database, spanning from 10/23/2020 to 10/23/2020.

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. Baxter Corporation's FEI number is 3000251214.

What types of violations has Baxter Corporation received?

Baxter Corporation 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 Baxter Corporation come from?

All FDA import refusal data for Baxter Corporation 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.