FDA Warning Letter — Nexera Medical, Inc.

Case 366878 — FEI 3008010722

The FDA took a Warning Letter action against Nexera Medical, Inc. on October 16, 2012 (Fort Lauderdale, FL). The action was issued by CDRH and concerns devices products. This facility has 4 recent FDA inspections on record.

Action Details

Facility
Nexera Medical, Inc.
Date
October 16, 2012
Fiscal Year
2013
Product Type
Devices
Center
CDRH
Location
Fort Lauderdale, FL (United States)