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General Project s.r.l.

⚠️ Moderate Risk

FEI: 3002952153 • Montespertoli, Florence • ITALY

FEI

FEI Number

3002952153

📍

Location

Montespertoli, Florence

🇮🇹

Country

ITALY
🏢

Address

Via Della Gora 15/19, , Montespertoli, Florence, Italy

Moderate Risk

FDA Import Risk Assessment

29.2
LowModerateHighCritical

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

Statistics

2
Total Refusals
4
Unique Violations
6/7/2013
Latest Refusal
8/6/2010
Earliest Refusal

Score Breakdown

Violation Severity
58.0×40%
Refusal Volume
17.7×30%
Recency
0.0×20%
Frequency
7.0×10%
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

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).

1261×

FAILS STD

The article appears to be a device which is subject to a performance standard established under Section 514 and does not appear to be in all respects in conformity with such standard.

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).

3411×

REGISTERED

It appears the device is subject to listing under 510(j) and the initial distributor has not registered as required by 21 CFR 807.20 (a)(5).

Refusal History

DateProductViolationsDivision
6/7/2013
79OLPOVER-THE-COUNTER POWERED RED/BLUE LIGHT BASED LASER FOR ACNE
118NOT LISTED
126FAILS STD
Florida District Office (FLA-DO)
8/6/2010
80LDQDEVICE, GENERAL MEDICAL
118NOT LISTED
237NO PMA
341REGISTERED
Seattle District Office (SEA-DO)

Frequently Asked Questions

What is General Project s.r.l.'s FDA import refusal history?

General Project s.r.l. (FEI: 3002952153) has 2 FDA import refusal record(s) in our database, spanning from 8/6/2010 to 6/7/2013.

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. General Project s.r.l.'s FEI number is 3002952153.

What types of violations has General Project s.r.l. received?

General Project s.r.l. 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 General Project s.r.l. come from?

All FDA import refusal data for General Project s.r.l. 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.