FDA Inspection 917997 — Alphatec Spine, Inc.

Alphatec Spine, Inc. — FEI 2027467

The FDA completed an inspection of Alphatec Spine, Inc. on Mar 13, 2015 in Carlsbad, CA. The inspection was classified OAI (Official Action Indicated — regulatory and/or administrative actions are recommended). Product area: Devices.

Inspection Details

Classification
Official Action Indicated (OAI)
End Date
Mar 13, 2015
Fiscal Year
2015
Product Type
Devices
Project Area
Compliance: Devices
Location
Carlsbad, CA (United States)

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