FDA Inspection 1284918 — Pronia Medical Systems

Pronia Medical Systems — FEI 3028631080

The FDA completed an inspection of Pronia Medical Systems on Sep 10, 2025 in Lewisburg, PA. 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
Sep 10, 2025
Fiscal Year
2025
Product Type
Devices
Project Area
Postmarket Assurance: Devices
Location
Lewisburg, PA (United States)

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