FDA Warning Letter — Bellus Medical

Case 495955 — FEI 3010392991

The FDA took a Warning Letter action against Bellus Medical on September 13, 2016 (Johnson City, TN). The action was issued by CDRH and concerns devices products. This facility has 2 recent FDA inspections on record.

Action Details

Facility
Bellus Medical
Date
September 13, 2016
Fiscal Year
2016
Product Type
Devices
Center
CDRH
Location
Johnson City, TN (United States)