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FDA Inspection 1178933 — Atrium Medical Corporation

Atrium Medical Corporation — FEI 3011175548

The FDA completed an inspection of Atrium Medical Corporation on September 6, 2022 in Merrimack, NH. 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 6, 2022
Fiscal Year
2022
Product Type
Devices
Project Area
Postmarket Assurance: Devices
Location
Merrimack, NH (United States)

Facility

Other inspections at this facility

  • 1232907 (VAI Tue Nov 26 2024 00:00:00 GMT+0000 (Coordinated Universal Time))
  • 1117399 (OAI Mon Feb 10 2020 00:00:00 GMT+0000 (Coordinated Universal Time))
  • 1060821 (NAI Thu Aug 02 2018 00:00:00 GMT+0000 (Coordinated Universal Time))
  • 977679 (OAI Wed Jul 13 2016 00:00:00 GMT+0000 (Coordinated Universal Time))
  • 956620 (NAI Fri Jan 08 2016 00:00:00 GMT+0000 (Coordinated Universal Time))

Recent compliance actions

FDA data resources