Suzhou Hengxiang Import & Export Co., Ltd.
⚠️ Moderate Risk
FEI: 3003355284 • Suzhou, Jiangsu • CHINA
FEI Number
3003355284
Location
Suzhou, Jiangsu
Country
CHINAAddress
Bldg., 6 Xi Ring Rd; Hengshanzhen Wujiang, Suzhou, Jiangsu, China
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
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).
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.
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 |
|---|---|---|---|
| 8/5/2008 | 80FOZCATHETER, INTRAVASCULAR, SHORT TERM | Chicago District Office (CHI-DO) | |
| 7/30/2007 | 79GECBRUSH, SCRUB, OPERATING-ROOM | Chicago District Office (CHI-DO) | |
| 7/30/2007 | 79GENFORCEPS, GENERAL & PLASTIC SURGERY | Chicago District Office (CHI-DO) | |
| 7/30/2007 | 88KDTCONTAINER, SPECIMEN MAILER AND STORAGE | Chicago District Office (CHI-DO) | |
| 7/30/2007 | 80MRZACCESSORIES, PUMP, INFUSION | Chicago District Office (CHI-DO) | |
| 3/3/2005 | 80MQXNEEDLE, ACUPUNCTURE, SINGLE USE | 16DIRECTIONS | San Francisco District Office (SAN-DO) |
| 3/3/2005 | 80MQXNEEDLE, ACUPUNCTURE, SINGLE USE | 16DIRECTIONS | San Francisco District Office (SAN-DO) |
| 3/3/2005 | 80MQXNEEDLE, ACUPUNCTURE, SINGLE USE | 16DIRECTIONS | San Francisco District Office (SAN-DO) |
| 2/18/2005 | 80MQXNEEDLE, ACUPUNCTURE, SINGLE USE | San Francisco District Office (SAN-DO) | |
| 12/3/2002 | 73BWINEEDLE, ACUPUNCTURE | Los Angeles District Office (LOS-DO) |
Frequently Asked Questions
What is Suzhou Hengxiang Import & Export Co., Ltd.'s FDA import refusal history?
Suzhou Hengxiang Import & Export Co., Ltd. (FEI: 3003355284) has 10 FDA import refusal record(s) in our database, spanning from 12/3/2002 to 8/5/2008.
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. Suzhou Hengxiang Import & Export Co., Ltd.'s FEI number is 3003355284.
What types of violations has Suzhou Hengxiang Import & Export Co., Ltd. received?
Suzhou Hengxiang Import & Export Co., Ltd. has been cited for 4 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 Suzhou Hengxiang Import & Export Co., Ltd. come from?
All FDA import refusal data for Suzhou Hengxiang Import & Export Co., Ltd. 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.