FDA Inspection 651907 — Atrium Medical Corporation

Atrium Medical Corporation — FEI 3011175548

The FDA completed an inspection of Atrium Medical Corporation on Mar 15, 2010 in Merrimack, NH. The inspection was classified VAI (Voluntary Action Indicated — objectionable conditions or practices were found, but the agency is not prepared to take or recommend any administrative or regulatory action). Product area: Devices.

Inspection Details

Classification
Voluntary Action Indicated (VAI)
End Date
Mar 15, 2010
Fiscal Year
2010
Product Type
Devices
Project Area
Compliance: Devices
Location
Merrimack, NH (United States)

Sources: openFDA, FDA Data Dashboard, FDA.gov. Report a data issue: hello@regdatalab.com.