FDA Inspection 1203431 — Arrotek Medical Ltd
The FDA completed an inspection of Arrotek Medical Ltd on March 7, 2023 in Sligo. 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
- March 7, 2023
- Fiscal Year
- 2023
- Product Type
- Devices
- Project Area
- Compliance: Devices
- Location
- Sligo (Ireland)