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Technipak

⚠️ Moderate Risk

FEI: 3003519524 • Greeley, CO • UNITED STATES

FEI

FEI Number

3003519524

📍

Location

Greeley, CO

🇺🇸
🏢

Address

2414 4th Avenue, , Greeley, CO, United States

Moderate Risk

FDA Import Risk Assessment

28.1
LowModerateHighCritical

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

Statistics

2
Total Refusals
2
Unique Violations
11/19/2007
Latest Refusal
7/6/2005
Earliest Refusal

Score Breakdown

Violation Severity
55.0×40%
Refusal Volume
17.7×30%
Recency
0.0×20%
Frequency
8.4×10%
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).

4881×

HEALTH C

The article is subject to refusal of admission pursuant to Section 801(a)(3) in that it appears to be misbranded in that the label or labeling bears an unauthorized nutrient content/health claim.

Refusal History

DateProductViolationsDivision
11/19/2007
54YCA99VITAMIN, MINERAL, PROTEINS AND UNCONVENTIONAL DIETARY SPECIALITIES FOR HUMANS AND ANIMALS, N.E.C.
488HEALTH C
Cincinnati District Office (CIN-DO)
7/6/2005
64RBE18HUMAN GROWTH HORMONE (HORMONE)
118NOT LISTED
San Francisco District Office (SAN-DO)

Frequently Asked Questions

What is Technipak's FDA import refusal history?

Technipak (FEI: 3003519524) has 2 FDA import refusal record(s) in our database, spanning from 7/6/2005 to 11/19/2007.

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. Technipak's FEI number is 3003519524.

What types of violations has Technipak received?

Technipak 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 Technipak come from?

All FDA import refusal data for Technipak 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.