FDA Warning Letter — Replication Medical, Inc.

Case 96125 — FEI 3004641714

The FDA took a Warning Letter action against Replication Medical, Inc. on Jul 2, 2010 (Monmouth Junction, NJ). The action was issued by CDRH and concerns devices products. This facility has 3 recent FDA inspections on record.

Action Details

Facility
Replication Medical, Inc.
Date
Jul 2, 2010
Fiscal Year
2010
Product Type
Devices
Center
CDRH
Location
Monmouth Junction, NJ (United States)