Zhejiang Huahai Pharmaceutical
FDA Inspections Database

Zhejiang Huahai Pharmaceutical

FDA Inspections Database

U.S. FDA inspection classifications and citation records from the official FDA inspection database.

VAI · Voluntary Action IndicatedNAI · No Action IndicatedOAI · Official Action Indicated China
  • Total Records 6
  • Latest Inspection 2024-11-20
  • Data Source U.S. FDA
  • Last Updated 2025-02-12
All
All
6
View records
NAI
No Action Indicated
3
View records
VAI
Voluntary Action Indicated
2
View records
OAI
Official Action Indicated
1
View records
Company Overview

Company

Zhejiang Huahai Pharmaceutical

Country

China

Website

Visit Website

Email

sales@huahaipharm.com

Company Snapshot

Zhejiang Huahai Pharmaceutical

Xunqiao, Linhai, Zhejiang 317024

China

en.huahaipharm.com:443/ sales@huahaipharm.com View on Map
FDA Inspections Timeline (6 records)
2024
20 Nov
Voluntary Action Indicated VAI

Legal Name

Zhejiang Huahai Pharmaceutical

Project Area

Drug Quality Assurance

Product Type

Drugs

Posted Citations

No

Inspection End Date

2024-11-20

FMD Date

2025-02-12

Fiscal Year

2025

State

Linhai, China

Location

Linhai, , China

Inspection Info

Fiscal Year: 2025
Citations: No

2021
29 Jul
No Action Indicated NAI

Legal Name

Zhejiang Huahai Pharmaceutical

Project Area

Drug Quality Assurance

Product Type

Drugs

Posted Citations

No

Inspection End Date

2021-07-29

FMD Date

2021-10-25

Fiscal Year

2021

State

Linhai, China

Location

Linhai, , China

Inspection Info

Fiscal Year: 2021
Citations: No

2018
03 Aug
Official Action Indicated OAI

Legal Name

Zhejiang Huahai Pharmaceutical

Project Area

Drug Quality Assurance

Product Type

Drugs

Posted Citations

No

Inspection End Date

2018-08-03

FMD Date

2021-11-04

Fiscal Year

2018

State

Linhai, China

Location

Linhai, , China

Inspection Info

Fiscal Year: 2018
Citations: No

2017
19 May
Voluntary Action Indicated VAI

Legal Name

Zhejiang Huahai Pharmaceutical

Project Area

Drug Quality Assurance

Product Type

Drugs

Posted Citations

No

Inspection End Date

2017-05-19

FMD Date

2017-09-15

Fiscal Year

2017

State

Linhai, China

Location

Linhai, , China

Inspection Info

Fiscal Year: 2017
Citations: No

2014
23 May
No Action Indicated NAI

Legal Name

Zhejiang Huahai Pharmaceutical

Project Area

Drug Quality Assurance

Product Type

Drugs

Posted Citations

No

Inspection End Date

2014-05-23

FMD Date

2014-08-13

Fiscal Year

2014

State

Linhai, China

Location

Linhai, , China

Inspection Info

Fiscal Year: 2014
Citations: No

2010
08 Sep
No Action Indicated NAI

Legal Name

Zhejiang Huahai Pharmaceutical

Project Area

Drug Quality Assurance

Product Type

Drugs

Posted Citations

No

Inspection End Date

2010-09-08

FMD Date

2011-04-12

Fiscal Year

2010

State

Linhai, China

Location

Linhai, , China

Inspection Info

Fiscal Year: 2010
Citations: No

Related Databases
  • FDA Inspections
    6 View
  • EDQM CEP
    49 View
  • KDMF
    0 View
  • Japan DMF
    0 View
  • Eudra GMP
    0 View
Official Source

All data is sourced from the official FDA inspection database maintained by the U.S. Food and Drug Administration.

Visit FDA.gov
Record Details Preview

Click "View Details" on any record above to expand full details inline.

Location

Linhai, , China

Inspection Info

Fiscal Year: 2025
Citations: No

100% Official Data

Directly from the U.S. FDA inspection database

Regular Updates

Data updated regularly from official sources

Trusted by Professionals

100K+ pharma professionals worldwide

Secure & Reliable

Enterprise-grade security and data protection

FDA inspection data is compiled from publicly available U.S. FDA inspection classification records.

Create a New Buying Request

Fields marked with * are mandatory.

Please enter quantity.
Please select a unit.
Please select quality standard.
Please select request type.
Please provide product specifications.
Please enter additional details.
Please select shipping preference.
Notice: By submitting this buying request, the provided product details and requirements may be published publicly on our marketplace.
Login to Submit