Home / Inspections / 930736

FDA Inspection 930736 — Datex-Ohmeda, Inc.

Datex-Ohmeda, Inc. — FEI 2112667

The FDA completed an inspection of Datex-Ohmeda, Inc. on June 12, 2015 in Madison, WI. 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
June 12, 2015
Fiscal Year
2015
Product Type
Devices
Project Area
Postmarket Assurance: Devices
Location
Madison, WI (United States)

Facility

Other inspections at this facility

  • 1223234 (VAI Fri Nov 17 2023 00:00:00 GMT+0000 (Coordinated Universal Time))
  • 1200471 (NAI Wed Mar 01 2023 00:00:00 GMT+0000 (Coordinated Universal Time))
  • 1169942 (NAI Wed May 04 2022 00:00:00 GMT+0000 (Coordinated Universal Time))
  • 1064872 (NAI Fri Aug 03 2018 00:00:00 GMT+0000 (Coordinated Universal Time))
  • 712376 (NAI Fri Jan 28 2011 00:00:00 GMT+0000 (Coordinated Universal Time))

FDA data resources