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Centre Biotechnique Avance

⚠️ Moderate Risk

FEI: 3006524914 • Albuquerque, NM • UNITED STATES

FEI

FEI Number

3006524914

📍

Location

Albuquerque, NM

🇺🇸
🏢

Address

1112 San Pedro Dr Ne, , Albuquerque, NM, United States

Moderate Risk

FDA Import Risk Assessment

26.3
LowModerateHighCritical

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

Statistics

1
Total Refusals
4
Unique Violations
11/7/2007
Latest Refusal
11/7/2007
Earliest Refusal

Score Breakdown

Violation Severity
55.0×40%
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).

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).

471×

NON STD

The article is subject to refusal of admission pursuant to section 536(a) of the Federal Food, Drug, and Cosmetic Act (FFDCA) in that it appears to be an electronic product offered for importation into the United States which fails to comply with an applicable standard prescribed pursuant to section 534 of the FFDCA.

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
11/7/2007
79GEXPOWERED LASER SURGICAL INSTRUMENTS
118NOT LISTED
341REGISTERED
47NON STD
508NO 510(K)
New Orleans District Office (NOL-DO)

Frequently Asked Questions

What is Centre Biotechnique Avance's FDA import refusal history?

Centre Biotechnique Avance (FEI: 3006524914) has 1 FDA import refusal record(s) in our database, spanning from 11/7/2007 to 11/7/2007.

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. Centre Biotechnique Avance's FEI number is 3006524914.

What types of violations has Centre Biotechnique Avance received?

Centre Biotechnique Avance 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 Centre Biotechnique Avance come from?

All FDA import refusal data for Centre Biotechnique Avance 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.