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FDA Inspection 651907 — Atrium Medical Corporation

Atrium Medical Corporation — FEI 3011175548

The FDA completed an inspection of Atrium Medical Corporation on March 15, 2010 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
March 15, 2010
Fiscal Year
2010
Product Type
Devices
Project Area
Compliance: Devices
Location
Merrimack, NH (United States)

Facility

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Recent compliance actions

FDA data resources