FDA Warning Letter — NuVasive Inc

Case 392911 — FEI 3002980729

The FDA took a Warning Letter action against NuVasive Inc on March 12, 2013 (San Diego, CA). The action was issued by CDRH and concerns devices products. This facility has 5 or more recent FDA inspections on record.

Action Details

Facility
NuVasive Inc
Date
March 12, 2013
Fiscal Year
2013
Product Type
Devices
Center
CDRH
Location
San Diego, CA (United States)