Fujifilm Diosynth Biotechnologies USA Inc. vs Philips North America: FDA Enforcement Comparison

Philips North America has been the subject of 355 FDA enforcement/approval records tracked by Argus HQ, compared to 1 for Fujifilm Diosynth Biotechnologies USA Inc..

Fujifilm Diosynth Biotechnologies USA Inc.: 0 warning letters, 0 recalls, 0 approval records, 1 Form 483.

Philips North America: 0 warning letters, 355 recalls, 0 approval records, 0 Form 483s.

Side by side

Fujifilm Diosynth Biotechnologies USA Inc. — Warning letters0

Philips North America — Warning letters0

Fujifilm Diosynth Biotechnologies USA Inc. — Recalls0

Philips North America — Recalls355

Fujifilm Diosynth Biotechnologies USA Inc. — Approval records0

Philips North America — Approval records0

Fujifilm Diosynth Biotechnologies USA Inc. — Form 483s1

Philips North America — Form 483s0

Timeline

Fujifilm Diosynth Biotechnologies USA Inc.

Most recent FDA action: March 27, 2026

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Philips North America

Most recent FDA action: July 1, 2026

Full history →

Cite this comparison

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

"Fujifilm Diosynth Biotechnologies USA Inc. vs Philips North America: FDA Enforcement Comparison." Argus HQ, accessed August 27, 2026. https://argushq.ai/compare/fujifilm-diosynth-biotechnologies-usa-inc-vs-philips-north-america

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