FDA Warning Letter — MicroPort Orthopedics Inc.

Case 453299 — FEI 3010536692

The FDA took a Warning Letter action against MicroPort Orthopedics Inc. on Jun 17, 2015 (Arlington, TN). The action was issued by CDRH and concerns devices products. This facility has 3 recent FDA inspections on record.

Action Details

Facility
MicroPort Orthopedics Inc.
Date
Jun 17, 2015
Fiscal Year
2015
Product Type
Devices
Center
CDRH
Location
Arlington, TN (United States)