SHIJIAZHUANG DIMAN BIOTECH CO
⚠️ Moderate Risk
FEI: 3020982370 • Shijiazhuang • CHINA
FEI Number
3020982370
Location
Shijiazhuang
Country
CHINAAddress
A2 805 Jinma Building, , Shijiazhuang, , 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
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).
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).
RX DEVICE
The article is subject to refusal of admission pursuant to Section 801(a)(3) in that it is a prescription device that appears to not feature a prescription device legend as required by 21 CFR 801.109.
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.
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).
Refusal History
| Date | Product | Violations | Division |
|---|---|---|---|
| 3/28/2023 | 87MOZACID, HYALURONIC, INTRAARTICULAR | 237NO PMA | Division of Southeast Imports (DSEI) |
| 3/3/2023 | 79LMHIMPLANT, DERMAL, COLLAGEN FOR AESTHETIC USE | 508NO 510(K) | Division of Southeast Imports (DSEI) |
| 2/9/2023 | 79MDMINSTRUMENT, MANUAL, GENERAL SURGICAL | Division of West Coast Imports (DWCI) | |
| 2/6/2023 | 79LMHIMPLANT, DERMAL, COLLAGEN FOR AESTHETIC USE | Division of Southeast Imports (DSEI) | |
| 2/6/2023 | 60QDL07LIDOCAINE | 75UNAPPROVED | Division of Southeast Imports (DSEI) |
| 2/11/2022 | 79LMHIMPLANT, DERMAL, COLLAGEN FOR AESTHETIC USE | Division of Southeast Imports (DSEI) |
Frequently Asked Questions
What is SHIJIAZHUANG DIMAN BIOTECH CO's FDA import refusal history?
SHIJIAZHUANG DIMAN BIOTECH CO (FEI: 3020982370) has 6 FDA import refusal record(s) in our database, spanning from 2/11/2022 to 3/28/2023.
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. SHIJIAZHUANG DIMAN BIOTECH CO's FEI number is 3020982370.
What types of violations has SHIJIAZHUANG DIMAN BIOTECH CO received?
SHIJIAZHUANG DIMAN BIOTECH CO has been cited for 7 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 SHIJIAZHUANG DIMAN BIOTECH CO come from?
All FDA import refusal data for SHIJIAZHUANG DIMAN BIOTECH 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.