GIANTSUN POWER ELECTRONICS (VIETNAM) CO., LTD
Official US Food and Drug Administration (FDA) Establishment Registration & Device/Facility Listing dossier for GIANTSUN POWER ELECTRONICS (VIETNAM) CO., LTD (FEI 3022946813). 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.
Factory No. 6, Lot CN8, Thach That - Quoc Oai Industrial Park, Phung Xa Commune, Thach That District, Hanoi Ci
Hanoi Ha Noi, Vietnam (13100)
FEI Number: 3022946813
Registration No: 3022946813 • Status Code: 1 (Active)
Yange Wang
IHEALTH LABS, INC
Sunnyvale, CA (USA)
408-6638349
policy@ihealthlabs.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.
Proprietary / Commercial Brand Names on File
| Product Code | FDA Classification Name | Device Class | 21 CFR Regulation | 510(k) Exempt? |
|---|---|---|---|---|
| OCH | Oximeter, Infrared, Sporting, Aviation | Class 2 | 21 CFR 870.2700 | 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 GIANTSUN POWER ELECTRONICS (VIETNAM) CO., LTD (FEI 3022946813) + 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 GIANTSUN POWER ELECTRONICS (VIETNAM) CO., LTD (FEI 3022946813) 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 Vietnam
COMATRIX TECHNOLOGY VIETNAM COMPANY LIMITED
Ho Chi Minh City, Vietnam • Reg Yr 2026
DAI THANG GENERAL BUSINESS LTD
Ho Chi Minh City,, Vietnam • Reg Yr 2026
ONFU electronics Co., LTD.
Trang Bom Dong Nai, Vietnam • Reg Yr 2026
GLOBAL CASES (VIETNAM) CORPORATION LIMITED
TAN UYEN TOWN Binh Duong, Vietnam • Reg Yr 2027
Frequently Asked Questions: FEI 3022946813 (GIANTSUN POWER ELECTRONICS (VIETNAM) CO., LTD)
What is the FDA FEI Number for GIANTSUN POWER ELECTRONICS (VIETNAM) CO., LTD?
According to public US FDA Establishment Registration records, GIANTSUN POWER ELECTRONICS (VIETNAM) CO., LTD (Hanoi Ha Noi, Vietnam) is assigned FDA Facility Establishment Identifier (FEI) 3022946813 (Registration No. 3022946813) with registration year 2026.
Who is the designated US Agent for FEI 3022946813 (GIANTSUN POWER ELECTRONICS (VIETNAM) CO., LTD)?
The registered US Agent on file for FEI 3022946813 is Yange Wang (IHEALTH LABS, INC) located in Sunnyvale, CA. Importers should independently confirm active representation before filing CBP ACE entry.
Does an active FDA FEI registration guarantee that shipments from GIANTSUN POWER ELECTRONICS (VIETNAM) 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.