FDA Inspection 1210581 — Palliare, Ltd.

Palliare, Ltd. — FEI 3017590240

The FDA completed an inspection of Palliare, Ltd. on June 21, 2023 in Galway. 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
June 21, 2023
Fiscal Year
2023
Product Type
Devices
Project Area
Compliance: Devices
Location
Galway (Ireland)