FDA Inspection 1231715 — Oxavita SRL

Oxavita SRL — FEI 3016489995

The FDA completed an inspection of Oxavita SRL on Feb 2, 2024 in Buenos Aires. 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
Feb 2, 2024
Fiscal Year
2024
Product Type
Devices
Project Area
Compliance: Devices
Location
Buenos Aires (Argentina)

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