SHENZHEN ALLBEAUTY TECHNOLOGY CO., LTD
Official US Food and Drug Administration (FDA) Establishment Registration & Device/Facility Listing dossier for SHENZHEN ALLBEAUTY TECHNOLOGY CO., LTD (FEI 3014467408). Use this record to cross-check CBP ACE Affirmation of Compliance codes (`DEV` / `DFE` / `FEI`), verify the designated US Agent on file, and subscribe to automated Import Alert (DWPE) monitoring.
801, Building #13, 6th Industrial Zone, Mashantou Community,, Matian Street, Guangming District
Shenzhen City Guangdong, China (518106)
FEI Number: 3014467408
Registration No: 3014467408 • Status Code: 1 (Active)
Susan Anthoney-DeWet
FDA Regulatory Consultants, LLC
Fort Lauderdale, FL (USA)
954-6558846
sue@fdaregulatoryconsultant.com
Registered FDA Product Codes, Device Classes & Commercial Names
Cross-check your commercial invoice product descriptions against these active FDA product code filings to prevent NO_510K or UNAPPROVED_NEW_DRUG port holds.
| Product Code | FDA Classification Name | Device Class | 21 CFR Regulation | 510(k) Exempt? |
|---|---|---|---|---|
| OHS | Light Based Over The Counter Wrinkle Reduction | Class 2 | 21 CFR 878.4810 | Requires 510(k) / Check |
Download Normalized 5-Year Refusal, 483 & Recall Audit Workbook (.XLSX + CSV)
Includes all deduplicated overseas factory names, FEI/DUNS crosswalks, 5-year port refusal logs, plain-English statutory violation mappings, and FSVP supplier qualification templates ready for customs broker review.
- Full 5-year OASIS refusal history for SHENZHEN ALLBEAUTY TECHNOLOGY CO., LTD (FEI 3014467408) + category peers
- 21 CFR 1.505 Foreign Supplier Verification Program (FSVP) audit checklist tab
Instant Supplier Detention Webhook & Email Alert Monitor
Get an automated Slack/Webhook JSON payload and email alert within 15 minutes whenever FDA OASIS logs a new detention, Import Alert Red List addition, or Warning Letter for SHENZHEN ALLBEAUTY TECHNOLOGY CO., LTD (FEI 3014467408) before you wire your 70% balance payment.
Shipment Detained by FDA or Placed on Import Alert? Request Free 24h Detention Evaluation from Licensed US FDA Compliance Counsel
When FDA issues a Notice of FDA Action (Detention), importers typically have only 10 to 20 business days to file a Form FDA 766 relabeling application, submit an accredited private laboratory packet (PLAP), or petition for Import Alert Red List removal before CBP orders refusal and liquidated damages.
Other Verified FDA FEI Establishments in China
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ZHONGSHAN A&E MACHINERY INDUSTRY CO., LTD
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JOYKEY INDUSTRIAL (PINGHU) LIMITED
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ZHEJIANG MEDIUNION HEALTHCARE GROUP CO.,LTD
Ningbo Zhejiang, China • Reg Yr 2026
Hangzhou AllTest Biotech Co.,Ltd
Hangzhou Zhejiang, China • Reg Yr 2027
SHANGHAI YUEYUESHU WOMEN PRODUCTS CO.,LTD.
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Frequently Asked Questions: FEI 3014467408 (SHENZHEN ALLBEAUTY TECHNOLOGY CO., LTD)
What is the FDA FEI Number for SHENZHEN ALLBEAUTY TECHNOLOGY CO., LTD?
According to public US FDA Establishment Registration records, SHENZHEN ALLBEAUTY TECHNOLOGY CO., LTD (Shenzhen City Guangdong, China) is assigned FDA Facility Establishment Identifier (FEI) 3014467408 (Registration No. 3014467408) with registration year 2027.
Who is the designated US Agent for FEI 3014467408 (SHENZHEN ALLBEAUTY TECHNOLOGY CO., LTD)?
The registered US Agent on file for FEI 3014467408 is Susan Anthoney-DeWet (FDA Regulatory Consultants, LLC) located in Fort Lauderdale, FL. Importers should independently confirm active representation before filing CBP ACE entry.
Does an active FDA FEI registration guarantee that shipments from SHENZHEN ALLBEAUTY TECHNOLOGY CO., LTD will clear US Customs without detention?
No. An active FDA FEI number or establishment registration only confirms administrative listing in FDA FURLS. Shipments can still be detained at US ports under Detention Without Physical Examination (DWPE / Import Alerts) for labeling, 510(k), cGMP, or adulteration violations.