Philips North America has been the subject of 355 FDA enforcement/approval records tracked by Argus HQ, compared to 1 for Charles River Laboratories, Inc. DBA Charles River, Endosafe.
Charles River Laboratories, Inc. DBA Charles River, Endosafe: 0 warning letters, 0 recalls, 0 approval records, 1 Form 483.
Philips North America: 0 warning letters, 355 recalls, 0 approval records, 0 Form 483s.
Side by side
Charles River Laboratories, Inc. DBA Charles River, Endosafe — Warning letters0
Philips North America — Warning letters0
Charles River Laboratories, Inc. DBA Charles River, Endosafe — Recalls0
Philips North America — Recalls355
Charles River Laboratories, Inc. DBA Charles River, Endosafe — Approval records0
Philips North America — Approval records0
Charles River Laboratories, Inc. DBA Charles River, Endosafe — Form 483s1
Philips North America — Form 483s0
Timeline
Charles River Laboratories, Inc. DBA Charles River, Endosafe
Most recent FDA action: March 27, 2026
Full history →Cite this comparison
Pre-formatted for a story, footnote, or reference list:
"Charles River Laboratories, Inc. DBA Charles River, Endosafe vs Philips North America: FDA Enforcement Comparison." Argus HQ, accessed August 17, 2026. https://argushq.ai/compare/charles-river-laboratories-inc-dba-charles-river-endosafe-vs-philips-north-america
Source: FDA.gov (aggregated across Warning Letters, Recalls, Approvals, Form 483s) ↗