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Kunshan Jiehong Nonwoven Product Co., Ltd., Suzhou, China – FDA Inspections

Inspection records and compliance data for Kunshan Jiehong Nonwoven Product Co., Ltd. in Suzhou. 3 FDA inspections on record, last inspected November 21, 2019.

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Company Profile

This profile covers Kunshan Jiehong Nonwoven Product Co., Ltd. based in Suzhou, China.

FDA Inspection History

FDA inspections
3
OAI
0
VAI
1
NAI
2
Form 483s
0
Warning letters
0

First inspected January 23, 2014. Last inspected November 21, 2019.

Most cited issue areas

  • Acceptable supplier records, inadequate records1 inspection
  • Design validation - Risk analysis1 inspection
  • Identification procedures, Lack of or inadequate procedures1 inspection

FDA inspections (3)

DateResultFDA center(s)Insp. #
November 21, 2019NAIMedical Devices & Rad Health · Compliance: Devices1113686
November 6, 2018NAIMedical Devices & Rad Health · Compliance: Devices1074262
January 23, 2014VAIMedical Devices & Rad Health · Compliance: Devices868178
FDA documents

No Form 483s, Warning Letters or EIRs on record.

Related Companies (10)

Companies with similar regulatory profiles, compliance history, and operations.

Krell Precision (Yangzhou) Co Ltd
Allmed Medical Products Co., Ltd. (Dong Guan Factory)
Guangzhou Hymson Laser Technology Co. Ltd.
GMDASZ Manufacturing Co., Ltd.
Wujiang Jia Chen Acupuncture Devices Co., Ltd.
Chongqing Kanghua Ruiming S&T Co., Ltd.
Dongguan Prestige Sporting Goods Co., Ltd.
Jingmen Huasheng Asia Dynamics Sanitary Products Co.
Suzhou Suntop Laser Technology Co. Ltd.
Siyang Holymed Products Co., Ltd.
Company Information

Name

Kunshan Jiehong Nonwoven Product Co., Ltd.

FEI Number

3006437555

Address

No. 895 Xinle Road, Dianshanhuzhen Kunshan, Suzhou, China

Country

China

ID: 380e1972-b977-4ca1-a04d-b847a6c089c1

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