FDA Warning Letter — Philips Respironics, Inc.

Case 433257 — FEI 2518422

The FDA took a Warning Letter action against Philips Respironics, Inc. on June 30, 2014 (Murrysville, PA). The action was issued by CDRH and concerns devices products. This facility has 5 or more recent FDA inspections on record.

Action Details

Facility
Philips Respironics, Inc.
Date
June 30, 2014
Fiscal Year
2014
Product Type
Devices
Center
CDRH
Location
Murrysville, PA (United States)