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Daheng New Epoch Technology, Inc., Beijing, China – FDA Inspections

Inspection records and compliance data for Daheng New Epoch Technology, Inc. in Beijing. 3 FDA inspections on record (1 OAI), 1 Form 483, last inspected July 14, 2017.

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Company Profile

This profile covers Daheng New Epoch Technology, Inc. based in Beijing, China.

FDA Inspection History

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

First inspected July 19, 2013. Last inspected July 14, 2017.

Most cited issue areas

  • Lack of or inadequate procedures1 inspection

FDA inspections (3)

DateResultFDA center(s)Insp. #
July 14, 2017NAIMedical Devices & Rad Health · Radiation Control and Health Safety Act1019785
May 20, 2014NAIMedical Devices & Rad Health · Radiation Control and Health Safety Act886350
July 19, 2013OAIMedical Devices & Rad Health · Radiation Control and Health Safety Act842315
FDA documents

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

Related Companies (10)

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

Flextronics Medical Device Manufacturing(Shenzhen) Co., Ltd.
DONGGUAN SIMPLE INDUSTRIAL COMPANY LIMITED
Precision Plus China Limited
Jiangsu Guangda Medical Material Group Co., Ltd.
Aok Tooling Ltd
Beijing E-Plus 3D Technology Co. Ltd.
Shanghai Chien Ti Motor Co., Ltd.
Zhongshan Eletech Metals Elec Factory
Dongguan Hong De Medical Plastic Products Co. Ltd.
Suzhou Dukangning Medical Products Co., Ltd.
Company Information

Name

Daheng New Epoch Technology, Inc.

FEI Number

3008705657

Address

# A9 Shang Dixinxi Road, Shangdi Xinxilu Haidian, Beijing, China

Country

China

ID: 4a965991-55f9-40a9-ac16-27b028cae1b5

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