Philips North America has been the subject of 355 FDA enforcement/approval records tracked by Argus HQ, compared to 9 for GE Medical Systems Information Technologies Inc.
GE Medical Systems Information Technologies Inc: 0 warning letters, 9 recalls, 0 approval records, 0 Form 483s.
Philips North America: 0 warning letters, 355 recalls, 0 approval records, 0 Form 483s.
Side by side
GE Medical Systems Information Technologies Inc — Warning letters0
Philips North America — Warning letters0
GE Medical Systems Information Technologies Inc — Recalls9
Philips North America — Recalls355
GE Medical Systems Information Technologies Inc — Approval records0
Philips North America — Approval records0
GE Medical Systems Information Technologies Inc — Form 483s0
Philips North America — Form 483s0
Timeline
GE Medical Systems Information Technologies Inc
Most recent FDA action: August 12, 2026
Full history →Cite this comparison
Pre-formatted for a story, footnote, or reference list:
"GE Medical Systems Information Technologies Inc vs Philips North America: FDA Enforcement Comparison." Argus HQ, accessed August 27, 2026. https://argushq.ai/compare/ge-medical-systems-information-technologies-inc-vs-philips-north-america
Source: FDA.gov (aggregated across Warning Letters, Recalls, Approvals, Form 483s) ↗