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Grifols Canada Plasma Inc.

⚠️ Moderate Risk

FEI: 3002806622 • Winnipeg, Manitoba • CANADA

FEI

FEI Number

3002806622

📍

Location

Winnipeg, Manitoba

🇨🇦

Country

CANADA
🏢

Address

137 Innovation Dr, , Winnipeg, Manitoba, Canada

Moderate Risk

FDA Import Risk Assessment

36.3
LowModerateHighCritical

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

Statistics

1
Total Refusals
1
Unique Violations
2/27/2002
Latest Refusal
2/27/2002
Earliest Refusal

Score Breakdown

Violation Severity
80.0×40%
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

2371×

NO PMA

The article is subject to refusal of admission pursuant to Section 801(a)(3) in that the device appears to be a Class III device and does not appear to have in effect an approved application for premarket approval pursuant to Section 515 of the Act, or an exemption pursuant to Section 520(g)(1).

Refusal History

DateProductViolationsDivision
2/27/2002
88LDTREAGENT, GENERAL PURPOSE
237NO PMA
New Orleans District Office (NOL-DO)

Frequently Asked Questions

What is Grifols Canada Plasma Inc.'s FDA import refusal history?

Grifols Canada Plasma Inc. (FEI: 3002806622) has 1 FDA import refusal record(s) in our database, spanning from 2/27/2002 to 2/27/2002.

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. Grifols Canada Plasma Inc.'s FEI number is 3002806622.

What types of violations has Grifols Canada Plasma Inc. received?

Grifols Canada Plasma Inc. 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 Grifols Canada Plasma Inc. come from?

All FDA import refusal data for Grifols Canada Plasma Inc. 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.