FDA Inspection 938947 — Avita Medial Americas Llc

Avita Medial Americas Llc — FEI 3001452123

The FDA completed an inspection of Avita Medial Americas Llc on Aug 21, 2015 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
Aug 21, 2015
Fiscal Year
2015
Product Type
Devices
Project Area
Compliance: Devices
Location
Ventura, CA (United States)