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FDA Inspection 1062457 — Mindray DS USA, Inc.

Mindray DS USA, Inc. — FEI 2221819

The FDA completed an inspection of Mindray DS USA, Inc. on April 20, 2018 in Mahwah, NJ. The inspection was classified NAI (No Action Indicated — no objectionable conditions were found). Product area: Devices.

Inspection Details

Classification
No Action Indicated (NAI) (NAI)
End Date
April 20, 2018
Fiscal Year
2018
Product Type
Devices
Project Area
Postmarket Assurance: Devices
Location
Mahwah, NJ (United States)

Facility

Other inspections at this facility

  • 1251239 (NAI Thu Feb 22 2024 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))
  • 849828 (VAI Mon Sep 23 2013 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