FDA Warning Letter — Atrium Medical Corporation

Case 363780 — FEI 3011175548

The FDA took a Warning Letter action against Atrium Medical Corporation on Oct 11, 2012 (Merrimack, NH). The action was issued by CDRH and concerns devices products. This facility has 5 or more recent FDA inspections on record.

Action Details

Facility
Atrium Medical Corporation
Date
Oct 11, 2012
Fiscal Year
2013
Product Type
Devices
Center
CDRH
Location
Merrimack, NH (United States)

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