ImportRefusal LogoImportRefusal

Philips Consumer Lifestyle Bv-Drachten

⚠️ Moderate Risk

FEI: 3010359222 • Drachten, Friesland • NETHERLANDS

FEI

FEI Number

3010359222

📍

Location

Drachten, Friesland

🇳🇱
🏢

Address

Tussendiepen 4, , Drachten, Friesland, Netherlands

Moderate Risk

FDA Import Risk Assessment

36.6
LowModerateHighCritical

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

Statistics

8
Total Refusals
6
Unique Violations
1/23/2023
Latest Refusal
7/18/2016
Earliest Refusal

Score Breakdown

Violation Severity
48.8×40%
Refusal Volume
35.3×30%
Recency
26.4×20%
Frequency
12.3×10%
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

1187×

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).

32606×

NO ENGLISH

Required label or labeling appears to not be in English in violation of 21 C.F.R. 801.15(c)(1)

5085×

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.

32804×

FRNMFGREG

The article is subject to refusal of admission pursuant to section 801(a)(3) in that it appears to be misbranded as defined in section 502(o) of the FD&C Act. It appears that it was manufactured, prepared, propagated, compounded, or processed in an establishment not duly registered under section 510 of the Act.

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).

4761×

NO REGISTR

The article appears to be an electronic product that does not comply with an applicable standard as prescribed by Section 534 because no reporting has been provided as required by Section 537(b).

Refusal History

DateProductViolationsDivision
1/23/2023
79OHTLIGHT BASED OVER-THE-COUNTER HAIR REMOVAL
118NOT LISTED
3280FRNMFGREG
341REGISTERED
476NO REGISTR
508NO 510(K)
Division of West Coast Imports (DWCI)
2/20/2019
79OHTLIGHT BASED OVER-THE-COUNTER HAIR REMOVAL
118NOT LISTED
3260NO ENGLISH
3280FRNMFGREG
508NO 510(K)
Division of Southeast Imports (DSEI)
6/21/2017
80LDQDEVICE, GENERAL MEDICAL
118NOT LISTED
3260NO ENGLISH
508NO 510(K)
Division of Southeast Imports (DSEI)
5/30/2017
79OHTLIGHT BASED OVER-THE-COUNTER HAIR REMOVAL
118NOT LISTED
3260NO ENGLISH
Division of Southeast Imports (DSEI)
4/10/2017
79OHTLIGHT BASED OVER-THE-COUNTER HAIR REMOVAL
118NOT LISTED
3260NO ENGLISH
3280FRNMFGREG
Division of Southeast Imports (DSEI)
1/20/2017
79OHTLIGHT BASED OVER-THE-COUNTER HAIR REMOVAL
118NOT LISTED
3260NO ENGLISH
508NO 510(K)
Cincinnati District Office (CIN-DO)
1/4/2017
79OHTLIGHT BASED OVER-THE-COUNTER HAIR REMOVAL
118NOT LISTED
3260NO ENGLISH
508NO 510(K)
Cincinnati District Office (CIN-DO)
7/18/2016
79OHTLIGHT BASED OVER-THE-COUNTER HAIR REMOVAL
3280FRNMFGREG
Philadelphia District Office (PHI-DO)

Frequently Asked Questions

What is Philips Consumer Lifestyle Bv-Drachten's FDA import refusal history?

Philips Consumer Lifestyle Bv-Drachten (FEI: 3010359222) has 8 FDA import refusal record(s) in our database, spanning from 7/18/2016 to 1/23/2023.

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. Philips Consumer Lifestyle Bv-Drachten's FEI number is 3010359222.

What types of violations has Philips Consumer Lifestyle Bv-Drachten received?

Philips Consumer Lifestyle Bv-Drachten 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 Philips Consumer Lifestyle Bv-Drachten come from?

All FDA import refusal data for Philips Consumer Lifestyle Bv-Drachten 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.