OFFICIAL OPENFDA FEI RECORDFEI: 3008517993Reg Yr: 2027China (CN)

ZHEJIANG ORIENT GENE BIOTECH

Official US Food and Drug Administration (FDA) Establishment Registration & Device/Facility Listing dossier for ZHEJIANG ORIENT GENE BIOTECH (FEI 3008517993). 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.

Registered Facility Address

3787 East Yangguang Avenue, Dipu Street, Anji

Huzhou Zhejiang, China (313300)

FDA FURLS Identifiers

FEI Number: 3008517993

Registration No: 3008517993 • Status Code: 1 (Active)

Designated U.S. Agent21 CFR 807.40

JIANQIU FANG

Bunker Hill Village, TX (USA)

281-8571217

fang.bryan@yahoo.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

healgen

Product Code	FDA Classification Name	Device Class	21 CFR Regulation	510(k) Exempt?
CKA	Nadh Oxidation/Nad Reduction, Alt/Sgpt	Class 1	21 CFR 862.1030	Requires 510(k) / Check

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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 ZHEJIANG ORIENT GENE BIOTECH (FEI 3008517993) before you wire your 70% balance payment.

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Respond-By Deadline Priority Triage

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.

Your Full Name & Role (Required)

Include your name and title (e.g., “Sarah Chen, VP Supply Chain”).

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Work Email for 24h Legal Memo (Required)

Used strictly to deliver your conflict-free 24h FDA detention evaluation.

Please enter a valid corporate email address.

Importer Website or Amazon/Shopify Store URL (Required)

Include https:// so counsel can pre-screen product Intended Use claims.

Please enter a valid URL starting with https:// or http://.

CBP Entry Number or Supplier FEI # (Required)

Format: 10-digit FEI (e.g., 3008517993) or 11-char CBP Entry # (e.g., W94-8829104-3).

Enter a 5–24 character alphanumeric FEI number or CBP Entry number.

US Port of Detention

Select the FDA District / Port holding the cargo.

Primary Cited FDA Charge Code

Charge listed on your Notice of FDA Action.

Commercial Cargo Value at Risk

Determines Form 766 vs. PLAP economic viability.

Notice of FDA Action Summary & Respond-By Date (Optional)

Describe whether cargo is currently on hold in ITACS, whether private lab sampling has started, or if you need an Import Alert removal petition.

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Frequently Asked Questions: FEI 3008517993 (ZHEJIANG ORIENT GENE BIOTECH)

What is the FDA FEI Number for ZHEJIANG ORIENT GENE BIOTECH?

According to public US FDA Establishment Registration records, ZHEJIANG ORIENT GENE BIOTECH (Huzhou Zhejiang, China) is assigned FDA Facility Establishment Identifier (FEI) 3008517993 (Registration No. 3008517993) with registration year 2027.

Who is the designated US Agent for FEI 3008517993 (ZHEJIANG ORIENT GENE BIOTECH)?

The registered US Agent on file for FEI 3008517993 is JIANQIU FANG located in Bunker Hill Village, TX. Importers should independently confirm active representation before filing CBP ACE entry.

Does an active FDA FEI registration guarantee that shipments from ZHEJIANG ORIENT GENE BIOTECH 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.