FDA Inspection 945696 — Proxy Biomedical Ltd.

Proxy Biomedical Ltd. — FEI 3004859928

The FDA completed an inspection of Proxy Biomedical Ltd. on Oct 1, 2015 in Galway. The inspection was classified NAI (No Action Indicated — no objectionable conditions or practices were found during the inspection). Product area: Devices.

Inspection Details

Classification
No Action Indicated (NAI)
End Date
Oct 1, 2015
Fiscal Year
2016
Product Type
Devices
Project Area
Compliance: Devices
Location
Galway (Ireland)

Sources: openFDA, FDA Data Dashboard, FDA.gov. Report a data issue: hello@regdatalab.com.