FDA Inspection 1050610 — Avita Medial Americas Llc

Avita Medial Americas Llc — FEI 3001452123

The FDA completed an inspection of Avita Medial Americas Llc on Feb 23, 2018 in Ventura, CA. 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 23, 2018
Fiscal Year
2018
Product Type
Devices
Project Area
Compliance: Devices
Location
Ventura, CA (United States)