FDA Inspection 1296662 — Infusyn Therapeutics

Infusyn Therapeutics — FEI 3030198397

The FDA completed an inspection of Infusyn Therapeutics on Nov 20, 2025 in Hackettstown, NJ. The inspection was classified NAI (No Action Indicated — no objectionable conditions or practices were found during the inspection). Product area: Devices.

Inspection details

Classification
No Action Indicated (NAI)
End Date
Nov 20, 2025
Fiscal Year
2026
Product Type
Devices
Project Area
Compliance: Devices
Location
Hackettstown, NJ (United States)

Sources: openFDA, FDA Data Dashboard, FDA.gov. Report a data issue: hello@regdatalab.com.