Heidelberg Engineering GmbH vs PHILIPS MEDICAL SYSTEMS NEDERLAND B.V.: FDA Enforcement Comparison

PHILIPS MEDICAL SYSTEMS NEDERLAND B.V. has been the subject of 205 FDA enforcement/approval records tracked by Argus HQ, compared to 1 for Heidelberg Engineering GmbH.

Heidelberg Engineering GmbH: 0 warning letters, 1 recall, 0 approval records, 0 Form 483s.

PHILIPS MEDICAL SYSTEMS NEDERLAND B.V.: 0 warning letters, 205 recalls, 0 approval records, 0 Form 483s.

Side by side

Heidelberg Engineering GmbH — Warning letters0

PHILIPS MEDICAL SYSTEMS NEDERLAND B.V. — Warning letters0

Heidelberg Engineering GmbH — Recalls1

PHILIPS MEDICAL SYSTEMS NEDERLAND B.V. — Recalls205

Heidelberg Engineering GmbH — Approval records0

PHILIPS MEDICAL SYSTEMS NEDERLAND B.V. — Approval records0

Heidelberg Engineering GmbH — Form 483s0

PHILIPS MEDICAL SYSTEMS NEDERLAND B.V. — Form 483s0

Timeline

Heidelberg Engineering GmbH

Most recent FDA action: September 30, 2026

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PHILIPS MEDICAL SYSTEMS NEDERLAND B.V.

Most recent FDA action: August 19, 2026

Full history →

Cite this comparison

Pre-formatted for a story, footnote, or reference list:

"Heidelberg Engineering GmbH vs PHILIPS MEDICAL SYSTEMS NEDERLAND B.V.: FDA Enforcement Comparison." Argus HQ, accessed October 12, 2026. https://argushq.ai/compare/heidelberg-engineering-gmbh-vs-philips-medical-systems-nederland-b-v

Source: FDA.gov (aggregated across Warning Letters, Recalls, Approvals, Form 483s) ↗