FDA Inspection 1024145 — Cranial Technologies, Inc

Cranial Technologies, Inc — FEI 3000215614

The FDA completed an inspection of Cranial Technologies, Inc on Jun 14, 2017 in Chandler, AZ. 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
Jun 14, 2017
Fiscal Year
2017
Product Type
Devices
Project Area
Postmarket Assurance: Devices
Location
Chandler, AZ (United States)

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