FDA Inspection 977679 — Atrium Medical Corporation

Atrium Medical Corporation — FEI 3011175548

The FDA completed an inspection of Atrium Medical Corporation on Jul 13, 2016 in Merrimack, NH. The inspection was classified OAI (Official Action Indicated — regulatory and/or administrative actions are recommended). Product area: Devices.

Inspection Details

Classification
Official Action Indicated (OAI)
End Date
Jul 13, 2016
Fiscal Year
2016
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.