FDA Inspection 975462 — Proxy Biomedical Ltd.

Proxy Biomedical Ltd. — FEI 3004859928

The FDA completed an inspection of Proxy Biomedical Ltd. on June 10, 2016 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 10, 2016
Fiscal Year
2016
Product Type
Devices
Project Area
Compliance: Devices
Location
Galway (Ireland)