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ENVIRON SKIN CARE (PTY) LTD (Prev. Environ Cosmeceutics CC)

⚠️ Moderate Risk

FEI: 3004604751 • Cape Town, Western Cape • SOUTH AFRICA

FEI

FEI Number

3004604751

📍

Location

Cape Town, Western Cape

🇿🇦
🏢

Address

14 Jan Smuts Road, , Cape Town, Western Cape, South Africa

Moderate Risk

FDA Import Risk Assessment

37.0
LowModerateHighCritical

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

Statistics

20
Total Refusals
12
Unique Violations
3/16/2017
Latest Refusal
6/7/2004
Earliest Refusal

Score Breakdown

Violation Severity
51.9×40%
Refusal Volume
49.0×30%
Recency
0.0×20%
Frequency
15.7×10%
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

4826×

NUTRIT LBL

The article is subject to refusal of admission pursuant to Section 801(a)(3) in that it appears to be misbranded in that the label or labeling fails to bear the required nutrition information.

5084×

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.

1184×

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).

753×

UNAPPROVED

The article is subject to refusal of admission pursuant to Section 801(a)(3) in that it appears to be a new drug within the meaning of Section 201(p) without an approved New Drug Application (NDA).

2183×

LIST INGRE

The article is subject to refusal of admission pursuant to Section 801(a)(3) of the FD&C Act in that it appears to be misbranded within the meaning of Section 403(i)(2) of the FD&C Act in that it is fabricated from two or more ingredients and the label fails to bear the common or usual name of each such ingredient and/or the article purports to be a beverage containing vegetable or fruit juice, but does not bear a statement with appropriate prominence on the information panel of the total percentage of such fruit or vegetable juice contained in the food.

3243×

NO ENGLISH

The article is subject to refusal of admission pursuant to Section 801(a)(3) of the FD&C Act in that it appears to be misbranded within the meaning of Section 403(f) of the FD&C Act in that any word, statement, or other information required by or under the authority of the FD&C Act to appear on the label or labeling is not prominently placed thereon with such conspicuousness (as compared with other words, statements, designs, or devices, in the labeling) and in such terms as to render it likely to be read and understood by the ordinary individual under customary terms of purchase and use (for example, label contains information in two or more languages but fails to repeat all required information in both languages in accordance with 21 CFR 101.15(c)(2), or label fails to include all required information in English in accordance with 21 CFR 101.15(c)(1), except in the case of articles distributed solely in the Commonwealth of Puerto Rico or in a Territory where the predominant language is one other than English)).

4733×

LABELING

The article appears in violation of FPLA because of its placement, form and/or contents statement.

162×

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.

4711×

CSTIC LBLG

The labeling appears to fail to comply with cosmetic labeling requirements of Section 602(a), and/or (b), and/or (c), and as identified by 21 C.F.R. Part 701.

32801×

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.

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
3/16/2017
53LC01CLEANSING (COLD CREAMS, CLEANSING LOTIONS, LIQUIDS, PADS) (SKIN CARE PREPARATIONS)
471CSTIC LBLG
New Orleans District Office (NOL-DO)
12/14/2016
89EGJDEVICE, IONTOPHORESIS, OTHER USES
118NOT LISTED
3280FRNMFGREG
508NO 510(K)
Cincinnati District Office (CIN-DO)
7/31/2012
79GEDBRUSH, DERMABRASION, MANUAL
237NO PMA
New England District Office (NWE-DO)
6/20/2012
54YCE99VITAMIN, MINERAL, PROTEINS AND UNCONVENTIONAL DIETARY SPECIALITIES FOR HUMANS AND ANIMALS, N.E.C.
324NO ENGLISH
482NUTRIT LBL
New Orleans District Office (NOL-DO)
6/20/2012
54ACA01VITAMIN A
324NO ENGLISH
482NUTRIT LBL
New Orleans District Office (NOL-DO)
6/20/2012
54YCE99VITAMIN, MINERAL, PROTEINS AND UNCONVENTIONAL DIETARY SPECIALITIES FOR HUMANS AND ANIMALS, N.E.C.
324NO ENGLISH
482NUTRIT LBL
New Orleans District Office (NOL-DO)
6/20/2012
54YBY99VITAMIN, MINERAL, PROTEINS AND UNCONVENTIONAL DIETARY SPECIALITIES FOR HUMANS AND ANIMALS, N.E.C.
218LIST INGRE
482NUTRIT LBL
New Orleans District Office (NOL-DO)
6/20/2012
54YBY99VITAMIN, MINERAL, PROTEINS AND UNCONVENTIONAL DIETARY SPECIALITIES FOR HUMANS AND ANIMALS, N.E.C.
218LIST INGRE
482NUTRIT LBL
New Orleans District Office (NOL-DO)
6/20/2012
54YBH99VITAMIN, MINERAL, PROTEINS AND UNCONVENTIONAL DIETARY SPECIALITIES FOR HUMANS AND ANIMALS, N.E.C.
218LIST INGRE
482NUTRIT LBL
New Orleans District Office (NOL-DO)
6/20/2012
79KCWEPILATOR, HIGH FREQUENCY, NEEDLE-TYPE
118NOT LISTED
508NO 510(K)
New Orleans District Office (NOL-DO)
3/30/2012
80LDQDEVICE, GENERAL MEDICAL
508NO 510(K)
New England District Office (NWE-DO)
3/30/2012
80LDQDEVICE, GENERAL MEDICAL
508NO 510(K)
New England District Office (NWE-DO)
3/22/2012
79NABGAUZE/SPONGE, NONRESORBABLE FOR EXTERNAL USE
118NOT LISTED
341REGISTERED
New England District Office (NWE-DO)
1/7/2011
62HBL99ANTI-MICROBIAL N.E.C.
75UNAPPROVED
New England District Office (NWE-DO)
1/7/2011
62HBL99ANTI-MICROBIAL N.E.C.
16DIRECTIONS
75UNAPPROVED
New England District Office (NWE-DO)
1/7/2011
62HBL99ANTI-MICROBIAL N.E.C.
16DIRECTIONS
75UNAPPROVED
New England District Office (NWE-DO)
8/25/2009
66VBJ99MISCELLANEOUS PATENT MEDICINES, ETC.
473LABELING
San Francisco District Office (SAN-DO)
8/25/2009
66VBJ99MISCELLANEOUS PATENT MEDICINES, ETC.
473LABELING
San Francisco District Office (SAN-DO)
8/25/2009
66VBJ99MISCELLANEOUS PATENT MEDICINES, ETC.
473LABELING
San Francisco District Office (SAN-DO)
6/7/2004
66VBL99MISCELLANEOUS PATENT MEDICINES, ETC.
118NOT LISTED
Los Angeles District Office (LOS-DO)

Frequently Asked Questions

What is ENVIRON SKIN CARE (PTY) LTD (Prev. Environ Cosmeceutics CC)'s FDA import refusal history?

ENVIRON SKIN CARE (PTY) LTD (Prev. Environ Cosmeceutics CC) (FEI: 3004604751) has 20 FDA import refusal record(s) in our database, spanning from 6/7/2004 to 3/16/2017.

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. ENVIRON SKIN CARE (PTY) LTD (Prev. Environ Cosmeceutics CC)'s FEI number is 3004604751.

What types of violations has ENVIRON SKIN CARE (PTY) LTD (Prev. Environ Cosmeceutics CC) received?

ENVIRON SKIN CARE (PTY) LTD (Prev. Environ Cosmeceutics CC) has been cited for 12 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 ENVIRON SKIN CARE (PTY) LTD (Prev. Environ Cosmeceutics CC) come from?

All FDA import refusal data for ENVIRON SKIN CARE (PTY) LTD (Prev. Environ Cosmeceutics CC) 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.