Zhejiang Huayi Pharmaceutical Co., Ltd.
⚠️ Moderate Risk
FEI: 3003657871 • Jinhua, Zhejiang • CHINA
FEI Number
3003657871
Location
Jinhua, Zhejiang
Country
CHINAAddress
15 Shuanglin Road, Fotangzhen Yiwu, Jinhua, Zhejiang, 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
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.
DRUG GMPS
The article is subject to refusal of admission pursuant to Section 801(a)(3) in that the methods used in and controls used for the manufacture, processing, packing, or holding of drugs and other products do not appear to conform to current good manufacturing practices within the meaning of Section 501(a)(2)(B).
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).
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).
NEW VET DR
The article is subject to refusal of admission pursuant to Section 801(a)(3) of the Federal Food, Drug, and Cosmetic Act in that it appears to be a new animal drug that is unsafe within the meaning of Section 512(a) of the Federal Food, Drug, and Cosmetic Act as it is not the subject of an approved new animal drug application, conditionally approved new animal drug application, or index listing, and no investigational new animal drug exemption applies.
Refusal History
| Date | Product | Violations | Division |
|---|---|---|---|
| 4/15/2013 | 62KCZ10OMEPRAZOLE (ANTI-PERISTALTIC, ANTI-DIARRHEAL) | Seattle District Office (SEA-DO) | |
| 1/28/2005 | 61GIP84NORFLOXACIN (ANTI-BACTERIAL, PART II) (NOT ANTIBIOTIC) | 118NOT LISTED | Division of Southeast Imports (DSEI) |
| 10/18/2004 | 68BYS20ANTI-INFECTIVE USED MORE THAN 1 SPECIES | 27DRUG GMPS | Division of Southeast Imports (DSEI) |
| 6/2/2004 | 68BYS20ANTI-INFECTIVE USED MORE THAN 1 SPECIES | 27DRUG GMPS | Florida District Office (FLA-DO) |
| 5/29/2002 | 62KCS10OMEPRAZOLE (ANTI-PERISTALTIC, ANTI-DIARRHEAL) | 75UNAPPROVED | Philadelphia District Office (PHI-DO) |
| 4/16/2002 | 56YKS99ANTIBIOTIC N.E.C. | Southwest Import District Office (SWI-DO) |
Frequently Asked Questions
What is Zhejiang Huayi Pharmaceutical Co., Ltd.'s FDA import refusal history?
Zhejiang Huayi Pharmaceutical Co., Ltd. (FEI: 3003657871) has 6 FDA import refusal record(s) in our database, spanning from 4/16/2002 to 4/15/2013.
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. Zhejiang Huayi Pharmaceutical Co., Ltd.'s FEI number is 3003657871.
What types of violations has Zhejiang Huayi Pharmaceutical Co., Ltd. received?
Zhejiang Huayi Pharmaceutical Co., Ltd. has been cited for 5 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 Zhejiang Huayi Pharmaceutical Co., Ltd. come from?
All FDA import refusal data for Zhejiang Huayi Pharmaceutical 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.