ENVIRON SKIN CARE (PTY) LTD (Prev. Environ Cosmeceutics CC)
⚠️ Moderate Risk
FEI: 3004604751 • Cape Town, Western Cape • SOUTH AFRICA
FEI Number
3004604751
Location
Cape Town, Western Cape
Country
SOUTH AFRICAAddress
14 Jan Smuts Road, , Cape Town, Western Cape, South Africa
Moderate Risk
FDA Import Risk Assessment
This firm has a moderate history of FDA import refusals. Some attention may be warranted.
Statistics
Score Breakdown
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
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.
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.
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).
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).
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.
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)).
LABELING
The article appears in violation of FPLA because of its placement, form and/or contents statement.
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.
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.
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.
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).
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
| Date | Product | Violations | Division |
|---|---|---|---|
| 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 | 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. | New Orleans District Office (NOL-DO) | |
| 6/20/2012 | 54ACA01VITAMIN A | New Orleans District Office (NOL-DO) | |
| 6/20/2012 | 54YCE99VITAMIN, MINERAL, PROTEINS AND UNCONVENTIONAL DIETARY SPECIALITIES FOR HUMANS AND ANIMALS, N.E.C. | New Orleans District Office (NOL-DO) | |
| 6/20/2012 | 54YBY99VITAMIN, MINERAL, PROTEINS AND UNCONVENTIONAL DIETARY SPECIALITIES FOR HUMANS AND ANIMALS, N.E.C. | New Orleans District Office (NOL-DO) | |
| 6/20/2012 | 54YBY99VITAMIN, MINERAL, PROTEINS AND UNCONVENTIONAL DIETARY SPECIALITIES FOR HUMANS AND ANIMALS, N.E.C. | New Orleans District Office (NOL-DO) | |
| 6/20/2012 | 54YBH99VITAMIN, MINERAL, PROTEINS AND UNCONVENTIONAL DIETARY SPECIALITIES FOR HUMANS AND ANIMALS, N.E.C. | New Orleans District Office (NOL-DO) | |
| 6/20/2012 | 79KCWEPILATOR, HIGH FREQUENCY, NEEDLE-TYPE | 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 | 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. | New England District Office (NWE-DO) | |
| 1/7/2011 | 62HBL99ANTI-MICROBIAL N.E.C. | 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.