FDA Inspection 706307 — Pronia Medical Systems

Pronia Medical Systems — FEI 3007365807

The FDA completed an inspection of Pronia Medical Systems on Dec 28, 2010 in South Salem, NY. 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 28, 2010
Fiscal Year
2011
Product Type
Devices
Project Area
Compliance: Devices
Location
South Salem, NY (United States)

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