FDA Inspection 1012220 — Globus Medical, Inc.

Globus Medical, Inc. — FEI 3004142400

The FDA completed an inspection of Globus Medical, Inc. on November 29, 2016 in West Norriton, PA. The inspection was classified NAI (No Action Indicated — no objectionable conditions were found). Product area: Devices.

Inspection Details

Classification
No Action Indicated (NAI) (NAI)
End Date
November 29, 2016
Fiscal Year
2017
Product Type
Devices
Project Area
Compliance: Devices
Location
West Norriton, PA (United States)