FDA Warning Letter — Nexera Medical, Inc.

Case 59862 — FEI 3008010722

The FDA took a Warning Letter action against Nexera Medical, Inc. on May 11, 2009 (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
May 11, 2009
Fiscal Year
2009
Product Type
Devices
Center
CDRH
Location
Fort Lauderdale, FL (United States)