PHILIPS MEDICAL SYSTEMS NEDERLAND B.V. has been the subject of 205 FDA enforcement/approval records tracked by Argus HQ, compared to 1 for Waldemar Link GmbH & Co. KG (Mfg Site).
PHILIPS MEDICAL SYSTEMS NEDERLAND B.V.: 0 warning letters, 205 recalls, 0 approval records, 0 Form 483s.
Waldemar Link GmbH & Co. KG (Mfg Site): 0 warning letters, 1 recall, 0 approval records, 0 Form 483s.
Side by side
PHILIPS MEDICAL SYSTEMS NEDERLAND B.V. — Warning letters0
Waldemar Link GmbH & Co. KG (Mfg Site) — Warning letters0
PHILIPS MEDICAL SYSTEMS NEDERLAND B.V. — Recalls205
Waldemar Link GmbH & Co. KG (Mfg Site) — Recalls1
PHILIPS MEDICAL SYSTEMS NEDERLAND B.V. — Approval records0
Waldemar Link GmbH & Co. KG (Mfg Site) — Approval records0
PHILIPS MEDICAL SYSTEMS NEDERLAND B.V. — Form 483s0
Waldemar Link GmbH & Co. KG (Mfg Site) — Form 483s0
Timeline
Cite this comparison
Pre-formatted for a story, footnote, or reference list:
"PHILIPS MEDICAL SYSTEMS NEDERLAND B.V. vs Waldemar Link GmbH & Co. KG (Mfg Site): FDA Enforcement Comparison." Argus HQ, accessed August 27, 2026. https://argushq.ai/compare/philips-medical-systems-nederland-b-v-vs-waldemar-link-gmbh-and-co-kg-mfg-site
Source: FDA.gov (aggregated across Warning Letters, Recalls, Approvals, Form 483s) ↗