ImportRefusal LogoImportRefusal

Majestic Aerotech Inc.

⚠️ Moderate Risk

FEI: 3003015706 • Eatontown, NJ • UNITED STATES

FEI

FEI Number

3003015706

📍

Location

Eatontown, NJ

🇺🇸
🏢

Address

542 Industrial Way W, , Eatontown, NJ, United States

Moderate Risk

FDA Import Risk Assessment

34.4
LowModerateHighCritical

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

Statistics

13
Total Refusals
3
Unique Violations
3/6/2008
Latest Refusal
12/3/2002
Earliest Refusal

Score Breakdown

Violation Severity
48.0×40%
Refusal Volume
42.5×30%
Recency
0.0×20%
Frequency
24.7×10%
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

11813×

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).

34110×

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).

5087×

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
3/6/2008
79LRRKIT, FIRST AID
118NOT LISTED
508NO 510(K)
New Orleans District Office (NOL-DO)
5/1/2003
80LYYGLOVE, PATIENT EXAMINATION, LATEX
118NOT LISTED
341REGISTERED
Chicago District Office (CHI-DO)
5/1/2003
73CAOAIRWAY, ESOPHAGEAL (OBTURATOR)
118NOT LISTED
341REGISTERED
Chicago District Office (CHI-DO)
5/1/2003
79GAXTOURNIQUET, NONPNEUMATIC
118NOT LISTED
341REGISTERED
Chicago District Office (CHI-DO)
3/31/2003
80LYYGLOVE, PATIENT EXAMINATION, LATEX
118NOT LISTED
508NO 510(K)
Chicago District Office (CHI-DO)
3/31/2003
73CAOAIRWAY, ESOPHAGEAL (OBTURATOR)
118NOT LISTED
508NO 510(K)
Chicago District Office (CHI-DO)
3/31/2003
80LYYGLOVE, PATIENT EXAMINATION, LATEX
118NOT LISTED
341REGISTERED
508NO 510(K)
Chicago District Office (CHI-DO)
3/31/2003
73CAOAIRWAY, ESOPHAGEAL (OBTURATOR)
118NOT LISTED
341REGISTERED
508NO 510(K)
Chicago District Office (CHI-DO)
3/31/2003
79GAXTOURNIQUET, NONPNEUMATIC
118NOT LISTED
341REGISTERED
Chicago District Office (CHI-DO)
3/31/2003
79GAXTOURNIQUET, NONPNEUMATIC
118NOT LISTED
341REGISTERED
Chicago District Office (CHI-DO)
3/19/2003
80LYYGLOVE, PATIENT EXAMINATION, LATEX
118NOT LISTED
341REGISTERED
508NO 510(K)
Chicago District Office (CHI-DO)
3/19/2003
73CAOAIRWAY, ESOPHAGEAL (OBTURATOR)
118NOT LISTED
341REGISTERED
508NO 510(K)
Chicago District Office (CHI-DO)
12/3/2002
79GAXTOURNIQUET, NONPNEUMATIC
118NOT LISTED
341REGISTERED
Chicago District Office (CHI-DO)

Frequently Asked Questions

What is Majestic Aerotech Inc.'s FDA import refusal history?

Majestic Aerotech Inc. (FEI: 3003015706) has 13 FDA import refusal record(s) in our database, spanning from 12/3/2002 to 3/6/2008.

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. Majestic Aerotech Inc.'s FEI number is 3003015706.

What types of violations has Majestic Aerotech Inc. received?

Majestic Aerotech Inc. has been cited for 3 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 Majestic Aerotech Inc. come from?

All FDA import refusal data for Majestic Aerotech Inc. 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.