Zhejiang Shenzhou Pharmaceutical Co.,Ltd. - NAI
FDA Inspections Database

Zhejiang Shenzhou Pharmaceutical Co.,Ltd. - NAI

FDA Inspections Database

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

NAI · No Action Indicated China
  • Total Records 3
  • Latest Inspection 2018-06-08
  • Data Source U.S. FDA
  • Last Updated 2018-10-17
All
All
5
View records
NAI
No Action Indicated
3
View records
VAI
Voluntary Action Indicated
2
View records
OAI
Official Action Indicated
0
No records
Company Overview

Company

Zhejiang Shenzhou Pharmaceutical Co.,Ltd. - NAI

Country

China

Website

Visit Website

Email

sales@shenzhoupharma.com

Company Snapshot

Zhejiang Shenzhou Pharmaceutical Co.,Ltd. - NAI

No 14 Chuancheng Nan Road, Xianju, Zhejiang 317300

China

www.shenzhoupharma.com/ sales@shenzhoupharma.com View on Map
FDA Inspections Timeline (3 records)
2018
08 Jun
No Action Indicated NAI

Legal Name

Zhejiang Shenzhou Pharmaceutical Co., Ltd.

Project Area

Drug Quality Assurance

Product Type

Drugs

Posted Citations

No

Inspection End Date

2018-06-08

FMD Date

2018-10-17

Fiscal Year

2018

State

Taizhou, China

Location

Taizhou, , China

Inspection Info

Fiscal Year: 2018
Citations: No

2013
18 Oct
No Action Indicated NAI

Legal Name

Zhejiang Shenzhou Pharmaceutical Co., Ltd.

Project Area

Drug Quality Assurance

Product Type

Drugs

Posted Citations

No

Inspection End Date

2013-10-18

FMD Date

2014-02-20

Fiscal Year

2014

State

Taizhou, China

Location

Taizhou, , China

Inspection Info

Fiscal Year: 2014
Citations: No

2011
08 Sep
No Action Indicated NAI

Legal Name

Zhejiang Shenzhou Pharmaceutical Co., Ltd.

Project Area

Drug Quality Assurance

Product Type

Drugs

Posted Citations

No

Inspection End Date

2011-09-08

FMD Date

-

Fiscal Year

2011

State

Taizhou, China

Location

Taizhou, , China

Inspection Info

Fiscal Year: 2011
Citations: No

Related Databases
  • FDA Inspections
    5 View
  • EDQM CEP
    4 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

Taizhou, , China

Inspection Info

Fiscal Year: 2018
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