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Sanipick Plastic

⚠️ Moderate Risk

FEI: 3010044251 • Spain • SPAIN

FEI

FEI Number

3010044251

📍

Location

Spain

🇪🇸

Country

SPAIN
🏢

Address

C/Carlos Jimenez Diaz 2328806 Alcala De, , Spain, , Spain

Moderate Risk

FDA Import Risk Assessment

29.9
LowModerateHighCritical

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

Statistics

4
Total Refusals
4
Unique Violations
2/4/2015
Latest Refusal
4/3/2013
Earliest Refusal

Score Breakdown

Violation Severity
50.0×40%
Refusal Volume
25.9×30%
Recency
0.0×20%
Frequency
21.7×10%
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

1184×

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).

32802×

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.

37411×

FRNMFGREG

The article is subject to refusal of admission pursuant to section 801(o) in that it is being imported or offered for import into the United States, and the importer, owner, or consignee of such article did not, at the time of offering the article for import, submit to the Secretary a statement that identifies the registration under section 510(i) of the Act of each establishment that with respect to such article is required under such section to register with the Secretary.

5081×

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.

Refusal History

DateProductViolationsDivision
2/4/2015
80MMKCONTAINER, SHARPS
118NOT LISTED
508NO 510(K)
Division of Southeast Imports (DSEI)
4/10/2013
80MMKCONTAINER, SHARPS
118NOT LISTED
3280FRNMFGREG
Division of Southeast Imports (DSEI)
4/10/2013
80MMKCONTAINER, SHARPS
118NOT LISTED
3280FRNMFGREG
Division of Southeast Imports (DSEI)
4/3/2013
80MMKCONTAINER, SHARPS
118NOT LISTED
3741FRNMFGREG
Division of Southeast Imports (DSEI)

Frequently Asked Questions

What is Sanipick Plastic's FDA import refusal history?

Sanipick Plastic (FEI: 3010044251) has 4 FDA import refusal record(s) in our database, spanning from 4/3/2013 to 2/4/2015.

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. Sanipick Plastic's FEI number is 3010044251.

What types of violations has Sanipick Plastic received?

Sanipick Plastic has been cited for 4 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 Sanipick Plastic come from?

All FDA import refusal data for Sanipick Plastic 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.