FDA Inspection 885654 — Globus Medical, Inc.

Globus Medical, Inc. — FEI 3004142400

The FDA completed an inspection of Globus Medical, Inc. on Jun 19, 2014 in West Norriton, PA. The inspection was classified VAI (Voluntary Action Indicated — objectionable conditions or practices were found, but the agency is not prepared to take or recommend any administrative or regulatory action). Product area: Devices.

Inspection Details

Classification
Voluntary Action Indicated (VAI)
End Date
Jun 19, 2014
Fiscal Year
2014
Product Type
Devices
Project Area
Postmarket Assurance: Devices
Location
West Norriton, PA (United States)

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