PHILIPS MEDICAL SYSTEMS NEDERLAND B.V. has been the subject of 199 FDA enforcement/approval records tracked by Argus HQ, compared to 4 for PHILIPS HEADQUARTERS CAMBRIDGE.
PHILIPS HEADQUARTERS CAMBRIDGE: 0 warning letters, 4 recalls, 0 approval records, 0 Form 483s.
PHILIPS MEDICAL SYSTEMS NEDERLAND B.V.: 0 warning letters, 199 recalls, 0 approval records, 0 Form 483s.
Side by side
PHILIPS HEADQUARTERS CAMBRIDGE — Warning letters0
PHILIPS MEDICAL SYSTEMS NEDERLAND B.V. — Warning letters0
PHILIPS HEADQUARTERS CAMBRIDGE — Recalls4
PHILIPS MEDICAL SYSTEMS NEDERLAND B.V. — Recalls199
PHILIPS HEADQUARTERS CAMBRIDGE — Approval records0
PHILIPS MEDICAL SYSTEMS NEDERLAND B.V. — Approval records0
PHILIPS HEADQUARTERS CAMBRIDGE — Form 483s0
PHILIPS MEDICAL SYSTEMS NEDERLAND B.V. — Form 483s0
Timeline
Cite this comparison
Pre-formatted for a story, footnote, or reference list:
"PHILIPS HEADQUARTERS CAMBRIDGE vs PHILIPS MEDICAL SYSTEMS NEDERLAND B.V.: FDA Enforcement Comparison." Argus HQ, accessed July 17, 2026. https://argushq.ai/compare/philips-headquarters-cambridge-vs-philips-medical-systems-nederland-b-v
Source: FDA.gov (aggregated across Warning Letters, Recalls, Approvals, Form 483s) ↗