ImportRefusal LogoImportRefusal

Erregierre S.p.A.

⚠️ Moderate Risk

FEI: 3002806924 • San Paolo d'Argon, Bergamo • ITALY

FEI

FEI Number

3002806924

📍

Location

San Paolo d'Argon, Bergamo

🇮🇹

Country

ITALY
🏢

Address

Via Francesco Baracca 19, , San Paolo d'Argon, Bergamo, Italy

Moderate Risk

FDA Import Risk Assessment

27.2
LowModerateHighCritical

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

Statistics

4
Total Refusals
7
Unique Violations
9/15/2011
Latest Refusal
4/11/2002
Earliest Refusal

Score Breakdown

Violation Severity
47.5×40%
Refusal Volume
25.9×30%
Recency
0.0×20%
Frequency
4.2×10%
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

28802×

RXCOMPOUND

the labeling fails to bear, at a minimum, the symbol "Rx only."

3332×

LACKS FIRM

The article is in package form and appears to not bear a label containing the name and place of business of the manufacturer, packer, or distributor.

3362×

INCONSPICU

Information required by the Act to be on the label or labeling does not appear to be conspicuous enough as to render it likely to be read and understood by the ordinary individual under customary conditions of purchase and use.

2232×

FALSE

The article is subject to refusal of admission pursuant to section 801(a)(3) in that it is a device whose labeling appears to be false or misleading.

1182×

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).

161×

DIRECTIONS

The article is subject to refusal of admission pursuant to section 801(a)(3) in that it is a device whose label appears to not bear adequate directions for use.

721×

NEW VET DR

The article is subject to refusal of admission pursuant to Section 801(a)(3) of the Federal Food, Drug, and Cosmetic Act in that it appears to be a new animal drug that is unsafe within the meaning of Section 512(a) of the Federal Food, Drug, and Cosmetic Act as it is not the subject of an approved new animal drug application, conditionally approved new animal drug application, or index listing, and no investigational new animal drug exemption applies.

Refusal History

DateProductViolationsDivision
9/15/2011
61WQA04CLOTRIMAZOLE (ANTI-FUNGAL) (NOT ANTIBIOTIC)
72NEW VET DR
New York District Office (NYK-DO)
9/29/2004
61NIR05BUPROPION HCL (ANTI-DEPRESSANT)
16DIRECTIONS
New York District Office (NYK-DO)
4/23/2002
62GCS99ANTI-INFLAMMATORY N.E.C.
118NOT LISTED
223FALSE
2880RXCOMPOUND
333LACKS FIRM
336INCONSPICU
Detroit District Office (DET-DO)
4/11/2002
62GCA99ANTI-INFLAMMATORY N.E.C.
118NOT LISTED
223FALSE
2880RXCOMPOUND
333LACKS FIRM
336INCONSPICU
Detroit District Office (DET-DO)

Frequently Asked Questions

What is Erregierre S.p.A.'s FDA import refusal history?

Erregierre S.p.A. (FEI: 3002806924) has 4 FDA import refusal record(s) in our database, spanning from 4/11/2002 to 9/15/2011.

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. Erregierre S.p.A.'s FEI number is 3002806924.

What types of violations has Erregierre S.p.A. received?

Erregierre S.p.A. has been cited for 7 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 Erregierre S.p.A. come from?

All FDA import refusal data for Erregierre S.p.A. 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.