Zhejiang Jinhua Conba Bio-Pharm. Co., Ltd. FDA Inspection Record

FEI 3003663281 · Inspections, Form 483s, warning letters and import refusals

Zhejiang Jinhua Conba Bio-Pharm. Co., Ltd. is an FDA-registered facility (FEI 3003663281) located in Zhejiang Province, CN. Registered operations: API MANUFACTURE; MANUFACTURE. RegDataLab tracks 5 FDA inspections at this facility.

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What FDA found at this site

Latest inspection
Apr 28, 2025: No Action Indicated (NAI)
Inspections on record
5 (3 VAI, 2 NAI)
Last OAI inspection
None on record
Warning letters
None matched to this FEI. Many letters do not state an FEI: search warning letters by company name
Form 483 and inspection documents
1 in FDA's reading room

A Form 483 lists an inspector's observations. OAI means FDA recommends regulatory and/or administrative action. A warning letter is FDA's formal enforcement notice. No record here does not establish that a site is safe. Check this site on FDA's Data Dashboard.

Inspections and what FDA cited

Newest first. Citations are the inspector observations FDA publishes for the inspection.

DateResultWhat FDA cited
Apr 28, 2025No Action Indicated (NAI)Cleaning / Sanitizing / Maintenance (21 CFR 211.67(a))
Dec 13, 2019No Action Indicated (NAI)No citations listed
Jan 26, 2018Voluntary Action Indicated (VAI)No citations listed
Oct 30, 2015Voluntary Action Indicated (VAI)No citations listed
Jan 23, 2013Voluntary Action Indicated (VAI)No citations listed

Form 483s and inspection documents

  • 483 on FDA.gov
    FDA listing date Aug 1, 2023, which is not always the inspection or issue date. Published by FDA Oct 20, 2026.

Facility details

Company
Zhejiang Jinhua Conba Bio-Pharm. Co., Ltd.
Location
Zhejiang Province (CN)
Registration Expires
Dec 31, 2026
Operations
API MANUFACTURE; MANUFACTURE
Source
decrs

Sources: openFDA, FDA Data Dashboard, FDA.gov. Report a data issue: hello@regdatalab.com.