PHILIPS MEDICAL SYSTEMS NEDERLAND B.V. has been the subject of 205 FDA enforcement/approval records tracked by Argus HQ, compared to 1 for PROD DEVELOPMENT.
PHILIPS MEDICAL SYSTEMS NEDERLAND B.V.: 0 warning letters, 205 recalls, 0 approval records, 0 Form 483s.
PROD DEVELOPMENT: 0 warning letters, 0 recalls, 1 approval record, 0 Form 483s.
Side by side
PHILIPS MEDICAL SYSTEMS NEDERLAND B.V. — Warning letters0
PROD DEVELOPMENT — Warning letters0
PHILIPS MEDICAL SYSTEMS NEDERLAND B.V. — Recalls205
PROD DEVELOPMENT — Recalls0
PHILIPS MEDICAL SYSTEMS NEDERLAND B.V. — Approval records0
PROD DEVELOPMENT — Approval records1
PHILIPS MEDICAL SYSTEMS NEDERLAND B.V. — Form 483s0
PROD DEVELOPMENT — Form 483s0
Timeline
Cite this comparison
Pre-formatted for a story, footnote, or reference list:
"PHILIPS MEDICAL SYSTEMS NEDERLAND B.V. vs PROD DEVELOPMENT: FDA Enforcement Comparison." Argus HQ, accessed August 27, 2026. https://argushq.ai/compare/philips-medical-systems-nederland-b-v-vs-prod-development
Source: FDA.gov (aggregated across Warning Letters, Recalls, Approvals, Form 483s) ↗