FDA Inspection 942944 — Caragh Precision

Caragh Precision — FEI 3009173317

The FDA completed an inspection of Caragh Precision on Sep 17, 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
Sep 17, 2015
Fiscal Year
2015
Product Type
Devices
Project Area
Postmarket Assurance: Devices
Location
Galway (Ireland)

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