FDA Warning Letter — Bausch Health Americas, Inc.

Case 509544 — FEI 3009443653

The FDA took a Warning Letter action against Bausch Health Americas, Inc. on November 3, 2016 (Rochester, NY). The action was issued by CDRH and concerns devices products. This facility has 5 or more recent FDA inspections on record.

Action Details

Facility
Bausch Health Americas, Inc.
Date
November 3, 2016
Fiscal Year
2017
Product Type
Devices
Center
CDRH
Location
Rochester, NY (United States)