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McGuff Company Inc.

⚠️ Moderate Risk

FEI: 3003189845 • Santa Ana, CA • UNITED STATES

FEI

FEI Number

3003189845

📍

Location

Santa Ana, CA

🇺🇸
🏢

Address

3524 W Lake Center Dr, , Santa Ana, CA, United States

Moderate Risk

FDA Import Risk Assessment

30.3
LowModerateHighCritical

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

Statistics

1
Total Refusals
2
Unique Violations
4/28/2014
Latest Refusal
4/28/2014
Earliest Refusal

Score Breakdown

Violation Severity
65.0×40%
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).

Refusal History

DateProductViolationsDivision
4/28/2014
54AFP13VITAMIN C (ASCORBIC ACID)
118NOT LISTED
27DRUG GMPS
Los Angeles District Office (LOS-DO)

Frequently Asked Questions

What is McGuff Company Inc.'s FDA import refusal history?

McGuff Company Inc. (FEI: 3003189845) has 1 FDA import refusal record(s) in our database, spanning from 4/28/2014 to 4/28/2014.

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. McGuff Company Inc.'s FEI number is 3003189845.

What types of violations has McGuff Company Inc. received?

McGuff Company Inc. 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 McGuff Company Inc. come from?

All FDA import refusal data for McGuff Company 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.