FDA Inspection 1060837 — Anteris Technologies Ltd
The FDA completed an inspection of Anteris Technologies Ltd on July 23, 2018 in Eagan, MN. The inspection was classified NAI (No Action Indicated — no objectionable conditions were found). Product area: Devices.
Inspection Details
- Classification
- No Action Indicated (NAI) (NAI)
- End Date
- July 23, 2018
- Fiscal Year
- 2018
- Product Type
- Devices
- Project Area
- Compliance: Devices
- Location
- Eagan, MN (United States)