FDA Warning Letter — Amplion Clinical Communications, Inc.

Case 416695 — FEI 3009164985

The FDA took a Warning Letter action against Amplion Clinical Communications, Inc. on December 17, 2013 (Nashville, TN). The action was issued by CDRH and concerns devices products. This facility has 5 or more recent FDA inspections on record.

Action Details

Facility
Amplion Clinical Communications, Inc.
Date
December 17, 2013
Fiscal Year
2014
Product Type
Devices
Center
CDRH
Location
Nashville, TN (United States)