FDA Inspection 1180328 — Anteris Technologies Ltd
The FDA completed an inspection of Anteris Technologies Ltd on August 16, 2022 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
- August 16, 2022
- Fiscal Year
- 2022
- Product Type
- Devices
- Project Area
- Postmarket Assurance: Devices
- Location
- Eagan, MN (United States)