FDA Inspection 1079173 — Globus Medical, Inc.

Globus Medical, Inc. — FEI 3011713200

The FDA completed an inspection of Globus Medical, Inc. on February 13, 2019 in Methuen, MA. The inspection was classified VAI (Voluntary Action Indicated — objectionable conditions were found but do not meet the threshold for regulatory action). 2 citations were issued during this inspection. Product area: Devices.

Inspection Details

Classification
Voluntary Action Indicated (VAI) (VAI)
End Date
February 13, 2019
Fiscal Year
2019
Product Type
Devices
Project Area
Compliance: Devices
Location
Methuen, MA (United States)

Citations

IDCFRDescription
328221 CFR 820.90(a)Nonconforming product, Lack of or inadequate procedures
369621 CFR 820.100(b)Documentation