FDA Warning Letter — Globus Medical, Inc.

Case 408025 — FEI 3004142400

The FDA took a Warning Letter action against Globus Medical, Inc. on Sep 26, 2013 (West Norriton, PA). The action was issued by CDRH and concerns devices products. This facility has 5 or more recent FDA inspections on record.

Action Details

Facility
Globus Medical, Inc.
Date
Sep 26, 2013
Fiscal Year
2013
Product Type
Devices
Center
CDRH
Location
West Norriton, PA (United States)

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