FDA Warning Letter — Brava, LLC

Case 432371 — FEI 3005643748

The FDA took a Warning Letter action against Brava, LLC on August 28, 2014 (Miami, FL). The action was issued by CDRH and concerns devices products. This facility has 4 recent FDA inspections on record.

Action Details

Facility
Brava, LLC
Date
August 28, 2014
Fiscal Year
2014
Product Type
Devices
Center
CDRH
Location
Miami, FL (United States)