SUN WAH (KEI KEE) MEDICINE CO
⚠️ Moderate Risk
FEI: 3017147196 • Sheung Wan, Hong Kong Island • HONG KONG
FEI Number
3017147196
Location
Sheung Wan, Hong Kong Island
Country
HONG KONGAddress
G/F, Heep Kee Commercial Building; 211 Wing Lok Street, Sheung Wan, Hong Kong Island, Hong Kong
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
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.
DIETARYLBL
The article is subject to refusal of admission pursuant to Section 801(a)(3) of the FD&C Act in that it is a dietary supplement that appears to be misbranded within the meaning of Section 403(s)(2)(B) of the FD&C Act in that the label or labeling fails to identify the product by using the term "dietary supplement", which term may be modified with the name of such an ingredient.
LACKS FIRM
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(e)(1) of the FD&C Act in that the food is in package form and the label fails to bear the name and place of business of the manufacturer, packer, or distributor.
NO ENGLISH
Required label or labeling appears to not be in English in violation of 21 C.F.R. 801.15(c)(1)
USUAL NAME
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)(1) of the FD&C Act in that the label fails to bear the common or usual name of the food, if any there be.
DIETARYING
The article is subject to refusal of admission pursuant to Section 801(a)(3) of the FD&C Act in that it is a dietary supplement that appears to be misbranded within the meaning of Section 403(s)(2)(A) of the FD&C Act in that the dietary supplement label or labeling fails to list the name of each dietary ingredient of the supplement and the quantity of each such dietary ingredient or , with respect to a proprietary blend of such dietary ingredients, the total quantity of all dietary ingredients in the blend.
NCONTACT
The article is subject to refusal of admission pursuant to Section 801(a)(3) of the FD&C Act in that it is a dietary supplement that appears to be misbranded within the meaning of Section 403(y) of the FD&C Act in that the dietary supplement label fails to bear a domestic address or phone number through which the responsible person (as described in section 761 of the FD&C Act) may receive a report of a serious adverse event with such dietary supplement.
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.
Refusal History
| Date | Product | Violations | Division |
|---|---|---|---|
| 6/9/2021 | 54EBT99HERBALS & BOTANICAL TEAS, N.E.C. | Division of Northeast Imports (DNEI) | |
| 6/9/2021 | 54EBT99HERBALS & BOTANICAL TEAS, N.E.C. | Division of Northeast Imports (DNEI) | |
| 6/9/2021 | 54EBT99HERBALS & BOTANICAL TEAS, N.E.C. | Division of Northeast Imports (DNEI) | |
| 6/9/2021 | 54EBT99HERBALS & BOTANICAL TEAS, N.E.C. | Division of Northeast Imports (DNEI) | |
| 6/9/2021 | 54EBT99HERBALS & BOTANICAL TEAS, N.E.C. | Division of Northeast Imports (DNEI) | |
| 6/9/2021 | 54EBT99HERBALS & BOTANICAL TEAS, N.E.C. | Division of Northeast Imports (DNEI) | |
| 6/9/2021 | 54EBT99HERBALS & BOTANICAL TEAS, N.E.C. | Division of Northeast Imports (DNEI) | |
| 6/9/2021 | 54EBT99HERBALS & BOTANICAL TEAS, N.E.C. | Division of Northeast Imports (DNEI) | |
| 6/9/2021 | 54EBT99HERBALS & BOTANICAL TEAS, N.E.C. | Division of Northeast Imports (DNEI) | |
| 6/9/2021 | 54EBT99HERBALS & BOTANICAL TEAS, N.E.C. | Division of Northeast Imports (DNEI) | |
| 6/9/2021 | 25LGH24GINGER ROOT, DRIED OR PASTE | Division of Northeast Imports (DNEI) | |
| 6/9/2021 | 54EBT99HERBALS & BOTANICAL TEAS, N.E.C. | Division of Northeast Imports (DNEI) | |
| 6/9/2021 | 54EBT99HERBALS & BOTANICAL TEAS, N.E.C. | Division of Northeast Imports (DNEI) | |
| 6/9/2021 | 54EBT99HERBALS & BOTANICAL TEAS, N.E.C. | Division of Northeast Imports (DNEI) |
Frequently Asked Questions
What is SUN WAH (KEI KEE) MEDICINE CO's FDA import refusal history?
SUN WAH (KEI KEE) MEDICINE CO (FEI: 3017147196) has 14 FDA import refusal record(s) in our database, spanning from 6/9/2021 to 6/9/2021.
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. SUN WAH (KEI KEE) MEDICINE CO's FEI number is 3017147196.
What types of violations has SUN WAH (KEI KEE) MEDICINE CO received?
SUN WAH (KEI KEE) MEDICINE CO has been cited for 8 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 SUN WAH (KEI KEE) MEDICINE CO come from?
All FDA import refusal data for SUN WAH (KEI KEE) MEDICINE CO 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.