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Mss Medical Supplies & Services

⚠️ Moderate Risk

FEI: 3008587619 • Keighley, West Yorkshire • UNITED KINGDOM

FEI

FEI Number

3008587619

📍

Location

Keighley, West Yorkshire

🇬🇧
🏢

Address

Unit 5, Business Park, Valley; Valley Road, Keighley, West Yorkshire, United Kingdom

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
6
Unique Violations
7/12/2011
Latest Refusal
7/12/2011
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).

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.

3361×

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.

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).

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.

841×

RX DEVICE

The article is subject to refusal of admission pursuant to Section 801(a)(3) in that it is a prescription device that appears to not feature a prescription device legend as required by 21 CFR 801.109.

Refusal History

DateProductViolationsDivision
7/12/2011
73CADVAPORIZER, ANESTHESIA, NON-HEATED
118NOT LISTED
16DIRECTIONS
336INCONSPICU
341REGISTERED
508NO 510(K)
84RX DEVICE
Los Angeles District Office (LOS-DO)

Frequently Asked Questions

What is Mss Medical Supplies & Services's FDA import refusal history?

Mss Medical Supplies & Services (FEI: 3008587619) has 1 FDA import refusal record(s) in our database, spanning from 7/12/2011 to 7/12/2011.

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. Mss Medical Supplies & Services's FEI number is 3008587619.

What types of violations has Mss Medical Supplies & Services received?

Mss Medical Supplies & Services has been cited for 6 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 Mss Medical Supplies & Services come from?

All FDA import refusal data for Mss Medical Supplies & Services 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.