Philips North America has been the subject of 355 FDA enforcement/approval records tracked by Argus HQ, compared to 1 for PROD DEVELOPMENT.
Philips North America: 0 warning letters, 355 recalls, 0 approval records, 0 Form 483s.
PROD DEVELOPMENT: 0 warning letters, 0 recalls, 1 approval record, 0 Form 483s.
Side by side
Philips North America — Warning letters0
PROD DEVELOPMENT — Warning letters0
Philips North America — Recalls355
PROD DEVELOPMENT — Recalls0
Philips North America — Approval records0
PROD DEVELOPMENT — Approval records1
Philips North America — Form 483s0
PROD DEVELOPMENT — Form 483s0
Timeline
Cite this comparison
Pre-formatted for a story, footnote, or reference list:
"Philips North America vs PROD DEVELOPMENT: FDA Enforcement Comparison." Argus HQ, accessed August 27, 2026. https://argushq.ai/compare/philips-north-america-vs-prod-development
Source: FDA.gov (aggregated across Warning Letters, Recalls, Approvals, Form 483s) ↗