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FDA Inspection 849828 — Mindray DS USA, Inc.

Mindray DS USA, Inc. — FEI 2221819

The FDA completed an inspection of Mindray DS USA, Inc. on September 23, 2013 in Mahwah, NJ. The inspection was classified VAI (Voluntary Action Indicated — objectionable conditions were found but do not meet the threshold for regulatory action). Product area: Devices.

Inspection Details

Classification
Voluntary Action Indicated (VAI) (VAI)
End Date
September 23, 2013
Fiscal Year
2013
Product Type
Devices
Project Area
Compliance: Devices
Location
Mahwah, NJ (United States)

Facility

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  • 1062457 (NAI Fri Apr 20 2018 00:00:00 GMT+0000 (Coordinated Universal Time))
  • 968103 (OAI Thu Mar 31 2016 00:00:00 GMT+0000 (Coordinated Universal Time))
  • 910764 (VAI Tue Mar 10 2015 00:00:00 GMT+0000 (Coordinated Universal Time))
  • 795266 (OAI Thu Aug 02 2012 00:00:00 GMT+0000 (Coordinated Universal Time))

Recent compliance actions

FDA data resources