FDA Inspection 918076 — HeartSine Technologies Ltd

HeartSine Technologies Ltd — FEI 3004123209

The FDA completed an inspection of HeartSine Technologies Ltd on Feb 12, 2015 in Belfast. 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
Feb 12, 2015
Fiscal Year
2015
Product Type
Devices
Project Area
Compliance: Devices
Location
Belfast (United Kingdom)

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