FDA Inspection 1259233 — Steris (Synergy Health Ede BV)

Steris (Synergy Health Ede BV) — FEI 3010223109

The FDA completed an inspection of Steris (Synergy Health Ede BV) on Dec 5, 2024 in Etten-Leur. 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
Dec 5, 2024
Fiscal Year
2025
Product Type
Devices
Project Area
Compliance: Devices
Location
Etten-Leur (Netherlands)

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